Unassociated Document
UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
10-K/A
(Amendment
No. 2)
(Mark
One)
x
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ANNUAL REPORT PURSUANT TO
SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF
1934
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For the
fiscal year ended: December
31,
2009
o
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TRANSITION REPORT PURSUANT
TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF
1934
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For the
transition period from ____________ to _________
Commission
file number: 001-34080
CHINA
SKY ONE MEDICAL, INC.
(Exact
name of registrant as specified in its charter)
Nevada
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87-0430322
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(State
or other jurisdiction of
incorporation
or organization)
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(I.R.S.
Employer
Identification
No.)
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No.
2158, North Xiang An Road, Song Bei District,
Harbin,
People’s Republic of China
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150028
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(Address
of principal executive offices)
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(Zip
Code)
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Registrant’s
telephone number, including area code:
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86-451-87032617
(China)
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Securities
registered pursuant to Section 12(b) of the Act:
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Title
of each class
None
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Name
of each exchange on which registered
Not
Applicable
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Securities
registered pursuant to Section 12(g) of the Act:
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Common
Stock
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(Title
of
Class)
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Indicate
by check mark if the registrant is a well-known seasonal issuer, as defined in
Rule 405 of the Securities Act.
Yes o No x
Indicate
by check mark if the registrant is not required to file reports pursuant to
Section 13 or Section 15(d) of the Act.
Yes o No
x
Indicate
by check mark whether the registrant (1) has filed all reports required to be
filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the
preceding 12 months (or for such shorter period that the registrant was required
to file such reports), and (2) has been subject to such filing requirements for
the past 90 days.
Yes x No
o
Indicate
by check mark whether the registrant has submitted electronically and posted on
its corporate Website, if any, every Interactive Data File required to be
submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this
chapter) during the preceding 12 months (or for such shorter period that
the registrant was required to submit and post such files).
Yes
o No
o
Indicate
by check mark if disclosure of delinquent filers pursuant to Item 405 of
Regulation S-K (§229.405 of this chapter) is not contained herein, and will not
be contained, to the best of registrant’s knowledge, in definitive proxy or
information statements incorporated by reference in Part III of this Form 10-K
or any amendment to this Form
10-K. o
Indicate
by check mark whether the registrant is a large accelerated filer, an
accelerated filer, a non-accelerated filer, or a small reporting
company. See the definitions of “large accelerated filer,”
“accelerated filer” and “smaller reporting company” in Rule 12b-2 of the
Exchange Act.
Large
accelerated filer o
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Accelerated
filer x
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Non-accelerated
filer o
(Do
not check if a smaller reporting company)
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Smaller
reporting company o
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Indicate
by check mark whether the registrant is a shell company (as defined in Rule
12b-2 of the Exchange Act).
Yes o No
x
As of
June 30, 2009, the aggregate market value of the voting and non-voting common
equity held by non-affiliates was approximately $135,214,631, based on the last
closing price of $13.48 per share, as quoted on the Nasdaq Global
Market.
As of
March 15, 2010, the registrant had 16,790,851 shares of common stock issued and
outstanding.
DOCUMENTS
INCORPORATED BY REFERENCE
None
EXPLANATORY
NOTE
This
Amendment No. 2 to the Annual Report on Form 10-K (“Amended Form 10-K”) of
China Sky One Medical, Inc. (the “Company”) amends the Company’s Annual Report
on Form 10-K for the year ended December 31, 2009, filed with the
Securities and Exchange Commission (“SEC”) on March 16, 2010, as previously
amended by the filing of a Form 10-K/A on March 17, 2010 (the “Form
10-K”).
As
announced in a Current Report on Form 8-K (the “Form 8-K”) the Company filed
with the SEC on May 11, 2010, on May 7, 2010, the Company’s management
determined that the Company’s previously filed financial statements for the
fiscal year ended December 31, 2009, included in the Form 10-K, should no longer
be relied upon due to an error in such financial statements with respect to the
accounting for certain derivative
instruments (warrants it issued in 2008 discussed below), which were previously
recorded as equity instruments in accordance with generally accepted accounting
principles in effect through December 31, 2008. The Company received
comments from the SEC, which led to management’s conclusion that the historical
financial statements in the Form 10-K require restatement to properly record
750,000 common stock purchase warrants, issued in connection with its January
31, 2008 private placement (the “Warrants”), as a derivative
liability.
The
Company has performed a complete assessment of the Warrants and has concluded
that the Warrants are within the scope of Accounting Standards Codification
815-40, “Derivatives and
Hedging – Contracts in Entity’s Own Equity” (“ASC 815-40”), formerly
Emerging Issues Task Force Issue No. 07-05, “Determining Whether an Instrument
(or Embedded Feature) Is Indexed to an Entity’s Own Stock” (“EITF
07-05”), due to the inclusion in the Warrants of a provision requiring a
weighted average adjustment to the exercise price of the Warrants in the event
the Company issues common stock, or securities convertible into or exercisable
for common stock, at a price per share lower than such exercise
price. Accordingly, ASC 815-40, formerly EITF 07-05, which was
effective as of January 1, 2009, should have been applied resulting in a
reclassification of the warrants as a derivative liability, measured at fair
value, with changes in fair value recognized as part of other income or expense
for each reporting period thereafter.
The
Company previously recorded a derivative liability of approximately $1.3 million
in connection with registration rights obligations with respect to securities
issued in the Company’s January 31, 2008 private placement. Also, on
May 7, 2010, the Company determined that, because the obligations do not require
a cash settlement and the Warrants can be settled in unregistered shares,
paragraphs 14-18 of EITF 00-19 do not apply to the registration rights
obligation. As a result, no liability is required to be recorded with
respect to this obligation and the Company is recharacterizing the $1.3 million
liability previously recorded as of December 31, 2009.
After
discussions with the Audit Committee of its Board of Directors and the Company’s
independent registered public accounting firm, management has determined to file
the Amended Form 10-K to reflect the corrections made in response to these
accounting errors. The correction of the errors impacts each of the
Company’s consolidated financial statements, but has no impact on the Company’s
income from operations or cash flows.
The
following tables ($ in thousands, except per share information) show the effects
of the restatement on the Company's consolidated balance sheet as of
December 31, 2009 and consolidated statements of operations and
comprehensive income:
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As of December 31, 2009
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As Previously
Recorded
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As Restated
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LIABILITIES
AND SHAREHOLDERS' EQUITY
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CURRENT
LIABILITIES
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Warrant
liability
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$ |
1,330 |
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$ |
11,435 |
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TOTAL
CURRENT LIABILITIES
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$ |
9,389 |
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$ |
19,494 |
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SHAREHOLDERS'
EQUITY
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Additional
paid in capital
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$ |
41,376 |
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$ |
37,188 |
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Retained
earnings
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$ |
83,702 |
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$ |
77,785 |
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TOTAL
SHAREHOLDERS' EQUITY
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$ |
130,974 |
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$ |
120,869 |
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TOTAL
LIABILITIES AND SHAREHOLDERS' EQUITY
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$ |
140,363 |
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$ |
140,363 |
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Year Ended December 31, 2009
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As Previously
Recorded
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As Restated
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INCOME
FROM OPERATIONS
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$ |
46,251 |
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$ |
46,251 |
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OTHER
INCOME (EXPENSE)
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Change
in fair value of derivative liability
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$ |
(1,330 |
) |
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$ |
(4,807 |
) |
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Total
other income (expense)
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$ |
(1,291 |
) |
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$ |
(4,768 |
) |
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INCOME
BEFORE PROVISION FOR INCOME TAXES
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$ |
44,960 |
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$ |
41,483 |
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NET
INCOME
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$ |
34,457 |
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$ |
30,980 |
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BASIC
EARNINGS PER SHARE
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$ |
2.08 |
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$ |
1.87 |
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DILUTED
EARNINGS PER SHARE
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$ |
2.07 |
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$ |
1.86 |
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COMPREHENSIVE
INCOME
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$ |
34,769 |
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$ |
31,292 |
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In
addition to the foregoing, in response to the SEC’s comments, the Company has
made additional revisions to the Form 10-K to enhance its disclosure regarding
its research and development activities and to provide additional information on
the income taxes of the Company. The Company also has corrected
certain typographical errors it discovered upon review of the Form
10-K
Except
as described above, no other amendments are being made to the Form
10-K. This Amended Form 10-K does not reflect events occurring after
the Form 10-K, or modify or update the disclosure contained therein in any other
way other than as required to reflect the amendments discussed
above.
The
Company has attached to this Amended Form 10-K updated certifications executed
as of the date of this Amended Form 10-K by the Chief Executive Officer and
Chief Financial Officer as required by Sections 302 and 906 of the Sarbanes
Oxley Act of 2002. These updated certifications are attached as
Exhibits 31.1, 31.2, 32.1 and 32.2 to this Amended Form 10-K.
CHINA
SKY ONE MEDICAL, INC.
ANNUAL
REPORT ON FORM 10-K
TABLE
OF CONTENTS
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PAGE
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Special
Note Regarding Forward-Looking Statements
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1
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PART
I
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2
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Item
1.
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Business
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2
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Item
1A.
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Risk
Factors
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16
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Item.
1B.
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Unresolved
Staff Comments
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30
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Item
2.
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Properties
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30
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Item
3.
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Legal
Proceedings
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30
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Item
4.
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Reserved
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30
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PART
II
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31
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Item
5.
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Market
for Registrant’s Common Equity, Related Stockholder Matters and Issuer
Purchases of Equity Securities
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31
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Item
6.
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Selected
Financial Data
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33
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Item
7.
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Management’s
Discussion and Analysis of Financial Condition and Results of
Operations
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34
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Item
7A.
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Quantitative
and Qualitative Disclosures About Market Risk
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50
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Item
8.
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Financial
Statements and Supplementary Data
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F-1
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Item
9.
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Changes
in and Disagreements With Accountants on Accounting and Financial
Disclosure
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52
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Item
9A.
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Controls
and Procedures
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52
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Item
9B.
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Other
Information
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53
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PART
III
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54
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Item10.
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Directors,
Executive Officers and Corporate Governance
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54
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Item
11.
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Executive
Compensation
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59
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Item
12.
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Security
Ownership of Certain Beneficial Owners and Management and Related
Stockholder Matters...
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64
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Item
13.
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Certain
Relationships and Related Transactions, and Director
Independence
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66
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Item
14.
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Principal
Accounting Fees and Services
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66
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Item
15.
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Exhibits,
Financial Statement Schedules
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67
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Signatures
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S-1
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SPECIAL
NOTE REGARDING FORWARD-LOOKING STATEMENTS
This
Annual Report on Form 10-K, together with other statements and information we
publicly disseminate, contains certain forward-looking statements within the
meaning of Section 27A of the Securities Act of 1933, as amended, and Section
21E of the Securities Exchange Act of 1934, as amended. We intend
such forward-looking statements to be covered by the safe harbor provisions for
forward-looking statements contained in the Private Securities Litigation Reform
Act of 1995, and include this statement for purposes of complying with these
safe harbor provisions.
Forward-looking
statements, which are based on certain assumptions and describe our future
plans, strategies and expectations, are generally identifiable by use of the
words “believe,” “expect,” “intend,” “anticipate,” “estimate,” “project” or
similar expressions. You should not rely on forward-looking
statements since they involve known and unknown risks, uncertainties and other
factors that are, in some cases, beyond our control and which could materially
affect actual results, performances or achievements.
Factors
that may cause actual results to differ materially from current expectations
include, but are not limited to the “Risk Factors” discussed in Part 1, Item 1A
of this Annual Report on Form 10-K. Accordingly, there is no
assurance that our expectations will be realized. Except as otherwise
required by the federal securities laws, we disclaim any obligations or
undertaking to publicly release any updates or revisions to any forward-looking
statement contained herein (or elsewhere) to reflect any change our expectations
with regard thereto, or any change in events, conditions or circumstances on
which any such statement is based.
The terms
“the Company,” “we,” “us” and “our” refer to China Sky One Medical, Inc.,
together with our consolidated subsidiaries.
PART
I
Item
1. Business.
General
We are
engaged, through our China-based indirect subsidiaries described below, in the
development, manufacture, marketing and sale of over-the-counter, branded
nutritional supplements and over-the-counter plant and herb-based pharmaceutical
and medicinal products. Our principal products are external use Traditional
Chinese Herbal Remedies/Medicines, commonly referred to in the industry as
“TCM.” We have evolved into an integrated manufacturer, marketer and
distributor of external-use TCM products sold primarily in the People’s Republic
of China (“China” or “PRC”) and through Chinese domestic pharmaceutical
chains. Recently, we have been expanding our worldwide sales effort
as well. Prior to 2009, we sold both our own manufactured products, as well as
medicinal and pharmaceutical products manufactured by others (the sale of third
party products is referred to herein as “Contract Sales”). Commencing
in 2009, we discontinued all of our Contract Sales as part of our revised
strategic plan.
Corporate
History
We are a
Nevada corporation formed on February 7, 1986, formerly known as Comet
Technologies, Inc. On July 26, 2006, after our acquisition of a
China-based nutritional supplements business, we changed our name to “China Sky
One Medical, Inc.” We are a holding company doing business through
American California Pharmaceutical Group, Inc., a California corporation
(“ACPG”), our non-operating United States (“U.S.”) holding company subsidiary,
and ACPG’s direct and indirect subsidiaries located in the People’s Republic of
China (the “PRC”).
ACPG, was
incorporated on December 16, 2003, under the name “QQ Group, Inc.” QQ
Group changed its name to “American California Pharmaceutical Group, Inc.” in
anticipation of the stock exchange transactions with our predecessor filer (then
known as “Comet Technologies, Inc.”) and Harbin City Tian Di Ren Medical Co., a
company organized under the laws of the PRC (“TDR”), as further described
below. On December 8, 2005, ACPG completed a stock exchange
transaction with TDR and TDR’s subsidiaries, each of which was a fully operating
company in the PRC. In connection with this transaction, ACPG
exchanged 100% of its issued and outstanding common stock for 100% of the
capital stock of TDR and its subsidiaries.
Thereafter,
on May 11, 2006, ACPG entered into a Stock Exchange Agreement (the “Exchange
Agreement”) with our shareholders. The transaction acquisition
contemplated under the Exchange Agreement was consummated on May 30,
2006. As a result of this transaction, we issued a total of
10,193,377 shares of our common voting stock to the stockholders of ACPG, in
exchange for 100% of the capital stock of ACPG. As a result, ACPG
became our wholly-owned subsidiary.
TDR was
originally formed in 1994 and its principal executive office is located in
Harbin City, Heilongjiang Province, PRC. On December 29, 2000, TDR
was reorganized and incorporated as a limited liability company under the
“Corporation Laws and Regulations” of the PRC. At the time of TDR’s
acquisition by ACPG, in December of 2005, TDR had two wholly-owned subsidiaries,
Harbin First Bio-Engineering Company Limited (“First”) and Kangxi
Medical Care Product Factory (“Kangxi”). In July, 2006, First and
Kangxi merged, with First as the surviving subsidiary of TDR.
As of
October 16, 2006, we organized Harbin Tian Qing Biotech Application Company as a
wholly-owned PRC subsidiary of TDR (“Tian Qing”), to conduct research and
development in the areas of tissue and stem cell banks, which is described in
further detail below. As of December 31, 2009, Tiang Qing had no
operating activities.
On April
3, 2008, TDR completed its acquisition of Heilongjiang Tianlong Pharmaceutical,
Inc., a company organized under the laws of the PRC (“Tianlong”), that has a
variety of medicines approved by the PRC’s State Food and Drug
Administration (the “SFDA”) and new medicine applications, and which is in the
business of manufacturing external-use pharmaceuticals. TDR
previously acquired the Beijing sales office of Tianlong in
mid-2006. In connection with this transaction, TDR acquired 100% of
the issued and outstanding capital stock of Tianlong from its sole stockholder,
in consideration for an aggregate purchase price of approximately $8,300,000,
consisting of $8,000,000 in cash, and 23,850 shares of our common stock (valued
at $12.00 per share).
On April
18, 2008, TDR consummated its acquisition of Heilongjiang Haina Pharmaceutical
Inc., a company organized under the laws of the PRC (“Haina”), licensed as a
wholesaler of TCM, bio-products, medicinal devices, antibiotics and chemical
medicines. Haina did not have an established sales network and was
acquired for its primary asset, a Good Supply Practice (“GSP”) license (License
No. A-HLJ03-010), issued by the Heilongjiang Province office of the SFDA as of
December 21, 2006. The SFDA only issues such licenses to
pharmaceutical resellers that maintain certain quality control
standards. The GSP license will be up for renewal on January 29,
2012. In connection with this transaction, TDR acquired 100% of the
issued and outstanding capital stock of Haina from its three stockholders in
consideration for payment of approximately $437,000.
On
September 5, 2008, TDR acquired Peng Lai Jin Chuang Pharmaceutical Company, a
company organized under the laws of the PRC (“Peng Lai ”), from its sole
stockholder. Peng Lai, which has received Good Manufacturing Practice
(“GMP”) certification from the SFDA, was organized to develop, manufacture and
distribute pharmaceutical, medicinal and diagnostic products in the
PRC. In connection with this transaction, TDR acquired all of Peng
Lai’s assets, including, without limitation, franchise, production and operating
rights to a portfolio of 20 medicines approved by the SFDA, for an aggregate
purchase price of approximately $7,000,000 million, consisting of approximately
$2,500,000 million in cash, and 381,606 shares of our common stock (valued at
$12.00 per share).
Principal
Products and Markets
We are
engaged, through TDR, and its subsidiaries in the PRC, in the development,
manufacture, marketing and sale of over-the-counter, branded nutritional
supplements and over-the-counter plant and herb-based pharmaceutical and
medicinal products. We have evolved into an integrated manufacturer,
marketer and distributor of external use Chinese medicine products sold
primarily to and through domestic pharmaceutical chains in the
PRC. Historically, we handled sales of both our own manufactured
products and Contract Sales of medicinal and pharmaceutical products
manufactured by others. However, commencing in 2009, we discontinued all
Contract Sales as part of our revised sales strategy.
With the
exception of Peng Lai, which is located in Shan Dong Province, PRC, all of our
manufacturing facilities are located in Heilongjiang Province,
PRC. In addition, we have sales offices located in 24 provinces
across China.
Our
principal products are external use TCMs. Using various formulas, we produce a
number of TCM products with several forms of delivery including ointments,
sprays, medicated skin patches, injections, capsules, suppositories, tablets and
granules. We also develop and sell bio-engineering products in the
form of diagnostic kits, which are used for testing for
different diseases. Over the next few years, we intend to concentrate
much of our efforts on the development, production and sales of TCM products and
testing kits, and antibiotic products.
Our
principal operations are in the PRC, where TDR and its subsidiaries have
manufacturing facilities and sales distribution channels covering most of the
provinces in the PRC. Part of our sales strategy is to expand our
worldwide sales by locating qualified distributors and sales agents outside of
the PRC. Our overall revenues were approximately $130,092,000 in
2009, of which export overseas sales were approximately $10,121,000, accounting
for approximately 7.8% of our total revenue. Overseas sales were
$7,570,000 in 2008, accounting for approximately 8.2% of our total
revenues. Overseas sales were $12,404,000 in 2007, accounting for
approximately 25.2% of our total revenue in 2007.
All of
our significant operations and long lived assets are located in the PRC. Below
is a chart depicting our corporate organizational structure:
SFDA
Licenses
The SFDA
issues the licenses to manufacture and market pharmaceutical products in the
PRC. Our licenses relate primarily to pharmaceutical production
licenses, which are needed mainly for topical products, ointments and external
test kits. TCM products also require a permit for sales, which permits are
generally granted on a non-exclusive basis for four to five years depending on
the product and subject to periodic review for renewal. For the year
ended December 31, 2009, we commercialized 91 products through TDR and its
subsidiaries. We have the necessary licenses and permits for all of
our products.
Our
TDR Subsidiary Owns the Following Subsidiaries in China
Harbin
First Bio-Engineering
On
September 26, 2003, TDR formed First under the laws of the PRC as its wholly
owned subsidiary, with an authorized capital of approximately $1,460,000
(10,000,000 RMB). First focuses on research and development of the
use of natural medicinal plants and biological technology products, such as our
diagnostic kits. First, which officially commenced production on July
21, 2006, is one of the first companies in Heilongjiang Province conducting
research and development of high technology biological products. First has
two product lines:
|
·
|
an
enzyme immunity reagent kit product line;
and
|
|
·
|
a
colloid gold product line.
|
Harbin
Tian Qing Biotech Application
On
October 16, 2006, TDR organized Tian Qing under the laws of the PRC as its
wholly owned subsidiary, to conduct research and development in the areas of
tissue and stem cell banks, which is described in more detail below. (See
“Research and Development” below.) As of December 31, 2009, Tian Qing
had no significant operations.
Heilongjiang
Tianlong Pharmaceutical
On April
3, 2008, TDR completed the acquisition of Tianlong, which is in the business of
manufacturing external-use pharmaceuticals. Tianlong’s assets
included, among other things, GMP certified manufacturing facilities,
state-of-the-art manufacturing equipment, a research and development center, and
production and operating rights to a portfolio of 69 medicines approved by the
SFDA.
Heilongjiang
Haina Pharmaceutical
On April
18, 2008, TDR consummated its acquisition of Haina, which is licensed as a
wholesaler of TCM, bio-products, medicinal devices, antibiotics and chemical
medicines. At the time of the acquisition, Haina did not have an
established sales network and was acquired for its primary asset, a GSP license
issued by the Heilongjiang Province office of the SFDA as of December 21,
2006. The SFDA only issues such licenses to resellers of medicines
that maintain certain quality control standards. The GSP license will
be up for renewal on January 29, 2012. Obtaining this license has
enabled us to expand our sales of medicinal products without having to go
through a lengthy license application process.
Peng
Lai Jin Chuang Pharmaceutical
On
September 5, 2008, TDR acquired Peng Lai, which received GMP certification from
the SFDA, and was organized to develop, manufacture and distribute
pharmaceutical products in the PRC. In connection with the
acquisition of Peng Lai , TDR acquired all of Peng Lai’s assets, including,
without limitation, franchise, production and operating rights to a
portfolio of 20 medicines approved by the SFDA.
Product
Line
In 2009,
we manufactured and marketed 91 products. Our manufacturing
operations are conducted in our indirect subsidiaries’ facilities located in
Heilongjiang Province and Shan Dong Province in the PRC.
For the
year ended December 31, 2009, we sold our products under five main
categories:
|
·
|
Ointments
(18 products);
|
|
·
|
Diagnostic
Kit (3 products);
|
A
description of our principle products, which generated a majority of our sales
revenue in 2009, is as follows:
Patch
Category:
Sumei
Slim Patch
The Sumei
Slim Patch is marketed and sold within and outside the PRC as a more natural
treatment to lose weight. The Sumei Slim Patch uses Saponin as its
major ingredient, and is effective in regulating and restraining the excessive
secretion of certain hormones, while promoting others to foster weight loss as
well as prevent weight gain.
Pain
Relief Patch
A pain
relief patch is designed to apply to the area of neck, shoulder, and
waist. The patch is used for a number of ailments, including fever,
headache, heart dysentery, diarrhea, and stiffness and pain caused by
hypertension.
Anti-Hypertension
Patch
The
anti-hypertension patch is based on five thousand years of Chinese herbal vein
therapy that has been adapted to a modern transdermal therapeutic system
(“TTS”). The product utilizes a Body-Yong-Guan point technique, which
is believed to maximize the effectiveness of the medicinal
ingredients. The product is believed to stimulate blood capillaries
and to be effective in improving circulation and reducing blood
pressure.
Ointment
Category:
Hemorrhoids
Ointment
This
product contains Acetate, Radix Notoginseng, and Rhizoma Coptidis. It
is made in soft ointment form that is effective in sterilizing and relieving
hemorrhoid symptoms, including itching, distending pain, burning, and
bleeding.
Compound
Camphor Cream
This
product is made for the treatment of various pathogens on the skin surface and
subcutaneously, such as mycete, trichopytic, staphylococcal bacteria aureus,
bacillus coli, and candida albicans (thrush).
Spray
Category:
Stomatitis
Spray
This
spray is used for the treatment of dental ulcers, pharyngitis, and
faucitis. It is made with pure herbal medicines and, thus,
has minimum side effects to human bodies.
Diagnostic
Kit Category:
Cardiac
Arrest Early Examination Kit
This
product is used for early stage diagnosis of myocardial infarction (heart
attacks).
Kidney
Disease Testing Kit
The
Urinate Micro Albumin Examination Testing Kit is used in connection with early
stage diagnosis for primary kidney disease, hypertension and
diabetes.
Other
Product Category:
We
include 48 of our products under the “Other” product category, because the
categories of applications for these products do not separately represent a
material amount of our revenues. The Other product category includes
suppositories, eye drops, nasal drops, capsules, granules, injections, tablets
and wash fluids.
Naftopidil
Dispersible Tablet
This
tablet is designed to treat benign enlargement of the prostate among males in
their middle age. It is effective in its treatment because its
ingredients can be easily digested and absorbed by the human body.
Naphazoline
Hydrochloride Eye Drop
Naphazoline
is recommended for the temporary relief of eye redness associated with minor
irritations. This product can comfort the eyes by lubricating them
and relieving such irritations.
Revenues
by Product Categories
We
believe that the most meaningful presentation of our products is by categories
of method of delivery. Our total revenues during fiscal 2009, 2008,
and 2007 were approximately $130,092,000, $91,816,000, and $49,318,000,
respectively. The following table sets forth our principal product
categories based on application type and the approximate amount and percentage
of revenue from each of such product categories for the fiscal years ended
December 31, 2009, 2008, and 2007:
|
|
For the Years Ended December 31
($ in thousands)
|
|
|
|
2009
|
|
|
2008
|
|
|
2007
|
|
Product Category
|
|
Sales
|
|
|
% of
Sales
|
|
|
Sales
|
|
|
% of
Sales
|
|
|
Sales
|
|
|
% of
Sales
|
|
Patches
|
|
$ |
40,770 |
|
|
|
31.3 |
% |
|
$ |
35,484 |
|
|
|
38.6 |
% |
|
$ |
19,609 |
|
|
|
39.9 |
% |
Ointments
|
|
|
28,862 |
|
|
|
22.2 |
% |
|
|
23,068 |
|
|
|
25.1 |
% |
|
|
3,270 |
|
|
|
12.6 |
% |
Sprays
|
|
|
18,499 |
|
|
|
14.2 |
% |
|
|
10,613 |
|
|
|
11.6 |
% |
|
|
8,742 |
|
|
|
18.7 |
% |
Diagnostic
Kits
|
|
|
10,239 |
|
|
|
7.9 |
% |
|
|
8,781 |
|
|
|
9.6 |
% |
|
|
2,994 |
|
|
|
6.1 |
% |
Contract
Sales
|
|
|
0 |
|
|
|
0.0 |
% |
|
|
5,655 |
|
|
|
6.2 |
% |
|
|
12,998 |
|
|
|
16.6 |
% |
Others
|
|
|
31,722 |
|
|
|
24.4 |
% |
|
|
8,215 |
|
|
|
8.9 |
% |
|
|
1,705 |
|
|
|
6.2 |
% |
Total
|
|
$ |
130,092 |
|
|
|
100.0 |
% |
|
$ |
91,816 |
|
|
|
100.0 |
% |
|
$ |
49,318 |
|
|
|
100.0 |
% |
For a
narrative description of the reasons for the changes in our revenue by
product category over the past three years, see “Management’s Discussion and
Analysis of Financial Condition and Results of Operations” below.
Research
and Development
We
conduct all of our research and development (“R&D”) activities either
internally or through collaborative arrangements with universities and research
institutions in the PRC. We have our own research, development and
laboratory facilities located in the facilities of First and
Tianlong. Our internal R&D team currently consists of 38
people. Many of our team members are professors affiliated with
universities in the PRC.
Additionally,
we have established several long-term partnerships with well-known universities
and enterprises in the PRC. We have:
|
·
|
Established
a gene medicine laboratory for Small RNA project with Harbin Medical
University; and
|
|
·
|
Established
a laboratory for Antroquinonol from Antrodia Camphorata with Taiwan Golden
Biotechnology Corporation.
|
Under our
partnership arrangements with universities and research institutions, we will
generally hold the intellectual property rights to any developed
technology. For example, as a result of our collaboration with Harbin
Medical University, a product known as “Endostatin” is currently under
development as a cancer suppressing product. Although this technology
still bears the name of Harbin Medical University, we own the intellectual
property rights pertaining to this technology. Additional information
relating to this product and other products being developed is set forth under
“Products Under Development” below and under the general product descriptions
throughout this report.
We
invested approximately $14,960,000, $7,413,000, and $3,158,000 in
R&D for the years ended December 31, 2009, 2008, and 2007,
respectively. Additional information about our R&D investments is
included in the financial statements in Item 8 of this report (and notes
thereto) and our “Management Discussion and Analysis on Financial Condition and
Results of Operations” section below.
Products
Under Development
The
projects which accounted for a majority of our 2009 research and development
expenses, grouped by subsidiary, are as follows:
TDR
Breast
Cancer Technology
Hyperplasie
Globulaire is the early stage of Hyperplasia of the Mammary Glands that has a
high occurrence among females between twenty-five and forty-five years of
age. Medicines with Endocrine can have significant side effects to
the patient. Our Breast Cancer Technology is designed to effectively
treat the Hyperplasie Globulaire with Traditional Chinese Medicine and with
minimum side effects. We spent approximately $2,272,000, or 15.2% of
total R&D expenditure in 2009, for efficacy testing, acute and long term
toxicity testing. This project is the only project that represented
more than 10% of our total R&D expenditures in 2009.
Monoclonal
Antibody Research
Monoclonal
antibody is a bioactive substance produced when human cells identify and resist
pathogenic intrusion from outside. Monoclonal antibody technology can
produce large amounts of pure antibodies with desired
substance. Tumor cells that can replicate endlessly are fused with
mammalian cells that produce an antibody. The result of this cell
fusion will continually produce antibodies. These antibodies are
called monoclonal because they come from only one type of cell, the hybridoma
cell. We believe Monoclonal antibodies have tremendous applications
in the field of diagnostics, therapeutics, targeted drug delivery systems, not
only for infectious disease caused by bacteria, viruses and protozoa, but also
for cancer, metabolic and hormonal disorders. We spent approximately
$965,000, or 6.5% of total R&D expenditure in 2009, for application
and performance appraisal. As of December 31, 2009, we
completed this project and are able to manufacture and commercialize these
antibody materials.
Endostatin
Research
Endostatin
is a cancer treatment drug that works by “starving” cancer cells by restricting
the generation of blood vessels around cancer lesions, thereby inhibiting, to a
degree, the source of nutrients upon which the cancer cells
survive. We have already completed teratogenicity testing, and have
established quality standards for this drug. Further
developments are underway to improve the product quality of
Endostatin. We spent approximately $439,000, or 2.9% of total R&D
expenditure in 2009, for acute and long term toxicity testing.
Patch
Products
We spent
approximately $1,820,000, or 12.2% of total R&D expenditure in 2009, for the
optimization experiments of several patch products including slim patch,
anti-hypertension patch, asthma patch, and pain relief patch. The
optimization experiments are focusing on optimization of the extracted
ingredients and irritation tests.
First
Diagnostic
Kits
In 2009,
we had 6 diagnostic kits under clinical trials. We spent
approximately $2,727,000, or 18.2% of total R&D expenditure in 2009, on
clinical trials for these 6 diagnostic kits.
Tianlong
Antroquinonol
Extracted from Antrodia Cinnamomea
Antrodia
Cinnamomea is well known in Taiwan as a traditional Chinese
medicine. For several decades, it has been used in the treatment of
food and drug intoxication, diarrhea, abdominal pain, hypertension, rashes, and
liver and lung cancer. We have obtained an exclusive right to develop this
technology with Taiwan Golden Biotechnology Corporation, which has completed
pre-clinical research on Antroquinonol in the United Kingdom. The
compound has been approved by the Food and Drug Administration in the U.S.
to enter into first stage clinical trial. We spent approximately
$387,000, or 2.6% of total R&D expenditure on this project in
2009.
Injections
In 2009,
we had 3 injections under clinical trials. We spent approximately
$1,944,000, or 13.1% of total R&D expenditure in clinical trials for these
projects in 2009.
Peng
Lai
We spent
an aggregate of approximately $879,000, or 5.9% of total R&D expenditure in
2009, in optimizing effectiveness test for Naftopidil Dispersible tablets for
prostate treatment, Sertraline Hydrochloride capsules for the treatment of
mental depression, and Radix Isatidis granules and syrup to treat Influenza
(flu).
Set
forth below is certain information regarding our major research and development
projects in 2009. The additional costs and expected completion dates
set forth in the table below are subject to change, which may be material, based
on various factors, many of which are out of our control:
Projects
|
|
Stage
|
|
2008 Expense
|
|
|
2009 Expense
|
|
|
Aggregate
Expenses Since
Commencement of
Project
|
|
|
Estimated
Additional Costs to
Complete Research
and Development
|
|
Remaining Activities and Expected Research and
Development Completion Date***
|
Diagnostic Kits -
19 products*
|
|
Clinical trial
|
|
$ |
2,261,000 |
|
|
$ |
2,727,000 |
|
|
$ |
4,988,000 |
|
|
|
$800,000 |
|
13
projects are estimated to be submitted to the SFDA in later half of 2010,
with an estimated aggregate cost of $500,000; Another 6 products are
estimated to complete clinical trial in fiscal 2010, then get into the
stage of long term stability testing through 2013, with estimated cost of
$300,000
|
Injections
- 6 projects
|
|
Clinical
trial
|
|
$ |
614,000 |
|
|
$ |
1,944,000 |
|
|
$ |
2,558,000 |
|
|
|
$300,000 |
|
One
product is pending SFDA approval; 3 products are planned to be submitted
to the SFDA within fiscal 2010, with an estimated cost of $100,000; The
other 2 products are going into long term stability testing stage with an
estimated cost of $200,000
|
Breast
Cancer Technology
|
|
Efficacy
testing, Acute and Long Term Toxicity testing
|
|
$ |
0 |
|
|
$ |
2,272,000 |
|
|
$ |
2,272,000 |
|
|
|
$8.3
million
|
|
Efficacy
stage has been completed in 2009, long term stability testing is estimated
to be completed during the first half of 2011, with an estimated cost of
$300,000, then apply to the SFDA for getting into the clinical trial. The
clinical trial is estimated to be completed in 2015, with an
estimated cost of $6-8 million, afterwards, we intend to apply to the SFDA
to enter into the production stage.
|
Patches
- 4 products
|
|
Extraction
optimization testing
|
|
$ |
0 |
** |
|
$ |
1,820,000 |
|
|
$ |
1,820,000 |
|
|
$ |
** |
Completed
|
Monoclonal
Antibody
|
|
Completed
|
|
$ |
948,000 |
|
|
$ |
965
,000 |
|
|
$ |
1,913,000 |
|
|
$1.8
to $2 million
|
|
Continue
study in 2010; does not require SFDA approval
|
Endostatin
|
|
Efficacy
testing, Acute and Long Term Toxicity testing
|
|
$ |
1,192,000 |
|
|
$ |
439,000 |
|
|
$ |
1,631,000 |
|
|
$8
to $10 million
|
|
Clinical
trials; estimated to be completed in 2016 and submitted for SFDA
approval
|
Antroquinonol
|
|
Clinical
trial
|
|
$ |
0 |
|
|
$ |
387,000 |
|
|
$ |
387,000 |
|
|
$16 to $18 million
|
|
Efficiency,
acute and long-term toxicity testing; pre-clinical and clinical trials are
estimated to be completed in 2018 and submitted for SFDA
approval
|
Radix
Isatidis granule and
syrup
|
|
Production
process optimization
|
|
$ |
0 |
|
|
$ |
282,000 |
|
|
$ |
282,000 |
|
|
|
$400,000 - $500,000 |
|
Estimated
to be completed in 2010
|
Naftopidil
Dispersible tablets
|
|
Production
process optimization
|
|
$ |
0 |
|
|
$ |
256,000 |
|
|
$ |
256,000 |
|
|
|
$400,000 - $500,000 |
|
Estimated
to be completed in 2010
|
Sertraline
Hydrochloride capsules
|
|
Production
process optimization
|
|
$ |
0 |
|
|
$ |
249,000 |
|
|
$ |
249,000 |
|
|
|
$400,000 - $500,000 |
|
Estimated
to be completed in
2010
|
* During
2008, we conducted long-term stability testing on clinical trials on a total of
13 projects for an aggregate expense of $2,261,000. We spent an
immaterial amount on further research and development of the projects in 2009
and expect to submit those projects for SFDA approval during the second half of
2010 at an estimated aggregate additional expense of
$500,000.
** The
amount is not meaningful.
*** Does
not include time required for SFDA approval, if any.
In
addition to the projects set forth in the table above, we commenced clinical
trials or efficacy, acute and long-term toxicity testing on several other
projects. We expect to complete testing and/or trials for these
projects between 2012 and 2014 at an estimated cost of $600,000 to $1,000,000
per project.
Total
research and development expenses in fiscal 2009 were
$14,960,000. The above listed projects comprise 75.6% of our total
research and development expenses in fiscal 2009. The other projects
and miscellaneous materials make up the remaining 24.2% of total research and
development expenses for the year.
Cord
Blood Stem Cell Bank
In 2006,
we began implementing a plan to establish a cord blood stem cell bank in the
PRC, for the treatment of various diseases such as leukemia, lymphoma and
rebirth anemia. On October 16, 2006, the Health Department of
Heilongjiang Province granted us, through Tian Qing, the exclusive right and
license to become engaged in tissue and stem cell bank activities in
Heilongjiang Province, PRC, through December 2010. Since the
development of this project will require substantial managerial, technical and
financial resources, and a number of significant risks, management is still
evaluating the proper timing and strategy in launching this
project.
Sales
Approach
Over the
past several years, we have continuously expanded our distribution channels for
our products. As a result, we have established a sales network
covering 24 provinces of mainland China, and have positioned sales managers and
representatives in each of these markets.
In fiscal
2007, our sales model was focused on the creation of our own distribution
channels. Therefore, we sold products directly to many small
distributors and retail store locations. Commencing in fiscal 2008,
we changed our business model and entered into distribution agreements with
larger regional sales agents, who resell to smaller distributors and retail
store locations. In addition, we entered into contracts with
nationwide chain pharmacies. These changes to our product
distribution channels resulted in our direct customer base decreasing from 943
customers at December 31, 2007 to 212 customers at December 31,
2009. Our change in sales strategy is further described in “Customers
and Distribution” below.
We also
managed to establish a marketing network through independent agents to develop
an international market for our products. At present, our primary
initial growth focus remains in the PRC. However, part of our sales
strategy is to expand our sales outside of the PRC. Overseas sales
accounted for approximately 7.8%, 8.2% and 25.2% of sales revenue for the fiscal
years ended December 31, 2009, 2008 and 2007, respectively.
Materials
and Suppliers
We employ
purchasing staff with extensive knowledge of our products, who work with our
marketing, product development, and formulations and quality control personnel
to source raw materials for our products and other items. Raw
materials are sourced principally in the PRC, and are generally available from a
variety of suppliers. Harbin Zhong Jia Medicine Company and
Heilongjiang Kangda Medicine Company accounted for approximately 16% and 42% of
our total inventory purchases for the year ended December 31, 2009,
respectively. Heilongjiang Kangda Medicine Company accounted for
approximately 33% of our total inventory purchases for the year ended December
31, 2008. Harbin Yong Heng accounted for 23% of our total inventory
purchases for the year ended December 31, 2007. No other suppliers
accounted for 10% or more of our total inventory purchases in 2009, 2008, and
2007.
We seek
to mitigate the risk of a shortage of raw materials, through identification of
alternative suppliers for the same or similar raw materials, where
available. We believe raw materials are available through alternative
suppliers in the market place, if necessary. We manufacture bulk
branded products to allow more extensive vertical integration and to improve the
quality and consistency of raw materials.
Historically,
we have signed agreements with suppliers that allowed us to hold extra raw
materials at the cost of the suppliers. As a result, we could
minimize our own inventory carrying costs, and improve our cash management, by
keeping the inventory at the minimum level required to support our short-term
sales. However, due to price increases for raw materials, and the
related overhead costs for storing such raw materials, we started to increase
our inventory levels toward the second half of 2009. In anticipation
of continued price increases, management may further increase our inventory
levels in fiscal 2010.
Customers
and Distribution
In fiscal
2007, our sales model was focused on the creation of our own distribution
channels. Therefore, we sold products directly to many small distributors and
retail store locations. In fiscal 2008, we changed our business model
and entered into distribution agreements with larger regional sales agents, who
resell to smaller distributors and retail store locations. In
addition, we entered into contracts with nationwide chain pharmacies. Through
the extensive sales networks, of these nationwide chains, we were able to reach
all major metropolitan areas throughout the PRC. These changes to our product
distribution channels resulted in our direct customer base decreasing from 943
customers at December 31, 2007 to 233 customers (not including branches of
retail and drug supply chains) at December 31, 2008. As of December
31, 2009, we had 212 customers, not including branches of retail and drug supply
chains.
The
change in our sales strategy, which began in fiscal 2008, was initiated to
improve product channel efficiencies, and to give us access to an increased
number of ultimate purchasers. We believe that these changes will
continue to lead to increased revenue by extending the reach of our distribution
network. By reducing the number of customers we sell to directly, we
have streamlined our accounts receivable management and collection and reduced
channel distribution costs. These favorable cost variances have been
partially offset by product price incentives we grant to the larger agents with
which we have contracted.
For the
year ended December 31, 2009, sales to Harbin Shiji Baolong Medicine Company and
Shanxi Xintai Medicine Company accounted for approximately 16% and 11% of total
revenues, respectively. Harbin Bao Da Medicine Company and Harbin
Shiji Baolong Medicine Company accounted for approximately 16% and 14% of our
accounts receivable in 2009, respectively. For the year ended
December 31, 2008, sales to Shanxi Xintai and Harbin Shiji Baolong accounted for
15% and 12% of our total revenues, respectively. Harbin Shiji Baolong
and Shanxi Xintai accounted for approximately 29% and 11% of our accounts
receivable in 2008, respectively. For the year ended December 31,
2007, sales to Ning BoYue Hua Trading Company and Guang Zhou Xing He Trading
Company accounted for approximately 14% and 11% of our total revenues,
respectively. Hua Li Jiu Zhou Company accounted for approximately 11%
of our accounts receivable in 2007. No other customers accounted for
10% or more of our total revenues or accounts receivable in 2009, 2008, and
2007.
In 2009,
we implemented various initiatives toward promoting and marketing our
products. Our advertising costs for the fiscal years ended December
31, 2009, 2008, and 2007 were approximately are $14,527,000, $7,299,000 and
$4,385,000, respectively.
We
will continue efforts to expand our markets into other provinces and larger
cities in the PRC, and to other markets worldwide. Currently, our
products are sold primarily in the PRC. In 2009, 2008 and 2007,
approximately 92.2%, 91.8% and 74.8% of our revenues were from the sale of
products in China, respectively. Part of our sales
strategy is to expand our worldwide sales. As a means of accelerating
our distribution into other countries, we will seek to enter into strategic
marketing arrangements with qualified firms that have distribution channels,
brand name recognition, or other unique marketing strengths.
Competition
Competition
in the TCM, pharmaceutical, and over-the-counter nutraceutical business is
intense in China, and throughout the world. We compete with various
firms, many of which produce and market products similar to our products, and
many of which have greater resources than us in terms of manufacturing and
marketing capabilities, management expertise and breadth, and financial
wherewithal. Some of these competitors are far larger, have more
resources then us and have stronger sales and distribution
networks.
Our
direct competitors are other domestic firms engaged in developing, manufacturing
and marketing TCM and nutraceutical products. There are many of these
companies in the PRC, in Heilongjiang Province, and even in the city of
Harbin.
We expect
that the competition for medicinal products in the PRC and other world markets
will become more intense over the next few years, both from existing
competitors, and new market entrants. We will also face competition
from foreign companies who may have established products, a strong proprietary
pipeline and strong financial resources. Our management believes that
we have certain competitive advantages in introducing new products to market
due to key focus areas for development, our existing distribution channels,
research and development capabilities and our relationship with certain
universities and other research institutions. However, there can be
no assurance that we will be able to compete and continue to grow in this highly
competitive environment. Additional information relating to
competition in the PRC can be found in the “Risk Factors” section
below.
Government
Regulation
Regulatory
Environment
Our
principal sales market is in the PRC. We are subject to the
Pharmaceutical Administrative Law of the PRC, which governs the licensing,
manufacturing, marketing and distribution of pharmaceutical products in the PRC,
and sets penalties for violations. Our business is subject to various
regulations and permit systems of the government of the
PRC. Additionally, we are subject to government licensing rights and
regulations, which relate to our stem cell R&D license. Permits
we attain for TCM products are granted on a non-exclusive basis and are subject
to periodical review for renewal.
The
governmental approval process in the PRC for a newly developed health product
can be lengthy and difficult. A product sample is first sent to a
clinical testing agent designated by the Ministry of Health, which conducts
extensive clinical testing and examination of the product to verify if it has
the specified functions as stated by the company producing the
product. A report will then be prepared and issued by the clinical
testing agent confirming or negating such functions. After
submittal to the agency, it generally takes six months to one year for a report
to be issued by the testing agent. The report must then be submitted
to a provincial Health Management Commission for approval. Following
this submittal, a letter of approval issued by such commission will be submitted
to the Ministry of Health for the issuance of a certificate that authorizes sale
and marketing of the product in the PRC.
This
entire process will generally take between eighteen months and two
years. The approval process will depend to a certain extent on
whether a specified product is a plant based pharmaceutical (“PBP”), or a plant
based nutraceutical (“PBN”). PBPs are products composed of herbs,
roots and plants that do not use synthetic chemicals, with certain medicinal
functions for treatment of one or more illnesses. PBPs are generally
prescription-based but in some cases may be sold
over-the-counter. PBNs, also frequently known as “dietary
supplements” or “nutritional supplements,” are also composed of herbs, roots and
plants, but are essentially prophylactic or preventive in nature. All
PBNs are available over-the-counter without a prescription. In the
PRC, PBPs require the approval of the SFDA, while PBNs only require the approval
of state and local governments prior to manufacturing and
sale. Obtaining the approval from the SFDA is generally more complex
and lengthy.
Because
we and our subsidiaries are wholly-owned enterprises, we are subject to the law
of foreign investment enterprises in the PRC, and the foreign company provisions
of the Company Law of China, which governs the conduct of our wholly-owned
subsidiaries and their officers and directors, and also limits our ability to
pay dividends.
Compliance
with Environmental Law
We comply
with the Environmental Protection Law of the PRC, as well as applicable local
regulations. In addition to compliance with the PRC law and local
regulations, we consistently undertake active efforts to ensure the
environmental sustainability of our operations. Because the
manufacturing of herb and plant-based products does not generally cause
significant damage or pollution to the environment, the cost of complying with
applicable environmental laws is not material. In the event we fail
to comply with applicable laws, we may be subject to penalties.
Intellectual
Property
We own
certain SFDA licenses for drug batch numbers and other proprietary
technologies. Historically, we included our proprietary
technologies and SFDA licenses for drug batch numbers within the category of
patents. We now believe it is more accurate to categorize such
intellectual property as SFDA licenses for drug batch numbers and other
proprietary technologies.
As of
December 31, 2009, our intellectual property breakdown by SFDA licenses for drug
batch numbers and other proprietary technologies is as follows:
IPs (Intangible Assets)
|
|
Year
Acquired
|
|
Acquisition
Cost
$ in thousands
|
|
|
Reflected under
Intangible
Assets
|
|
|
Proprietary
Technologies
|
|
|
Drug Batch
Numbers
|
|
Endostatin
|
|
2006
|
|
$ |
1,727 |
|
|
|
Yes
|
|
|
|
Yes |
|
|
|
- |
|
SFDA
licenses for drug batch numbers
|
|
2008
|
|
$ |
6,848 |
|
|
|
Yes
|
|
|
|
- |
|
|
|
Yes |
|
Monoclonal
Antibody
|
|
2008
|
|
$ |
5,106 |
|
|
|
Yes |
|
|
|
Yes |
|
|
|
- |
|
Breast
Cancer Technology
|
|
2008
|
|
$ |
1,459 |
|
|
|
Yes |
|
|
|
Yes |
|
|
|
- |
|
Antroquinonol
|
|
2009
|
|
$ |
5,119 |
|
|
|
Yes |
|
|
|
Yes |
|
|
|
- |
|
Small
RNAs Technology
|
|
2009
|
|
$ |
5,850 |
|
|
|
Yes |
|
|
|
Yes |
|
|
|
- |
|
We
purchased the rights to the patents for Endostatin and Antroquinonol, which are
registered under the names of Harbin Medical University and Taiwan Golden
Biotechnology Corporation, respectively.
We have
acquired certain additional proprietary technologies from non-related third
parties. The fair value of these proprietary technologies recorded in
our financial statements are appraised periodically and amortized during its
useful life.
As of the
date of this filing, we own two registered patents for product
packaging. As of December 31, 2009, these patents have nominal
carrying values.
Under the
PRC’s State Protection Law, certain herbal medicine products, which have
received approval from the SFDA, have automatic protection. SFDA
licenses for drug batch numbers we acquired in connection with our acquisitions
of Tianlong and Peng Lai in fiscal 2008 have been recorded as part of our
intangible assets. We did not appraise or assign any value to the
SFDA licenses for drug batch numbers developed internally by TDR or
First.
We have
registered “Kang Xi” as our trademark, which is used for all of our TCM
products. The “Kang Xi” trademark was developed internally and
registered by TDR before we became a public company. Our cost basis
in the trademark is nominal.
Employees
The
number of our employees has increased due to growth, increased research and
development activities and expanded marketing and distribution efforts for our
products. Our employees generally fall into the following
categories:
By
subsidiary company:
|
|
Number of Employees
|
|
Company
|
|
2009
|
|
|
2008
|
|
TDR
|
|
|
1,315 |
|
|
|
1,515 |
|
Tian
Qing
|
|
|
0 |
|
|
|
0 |
|
First
|
|
|
107 |
|
|
|
97 |
|
Tianlong
|
|
|
207 |
|
|
|
97 |
|
Haina
|
|
|
399 |
|
|
|
24 |
|
Peng
Lai
|
|
|
126 |
|
|
|
71 |
|
TOTAL:
|
|
|
2,154 |
|
|
|
1,804 |
|
By nature
of job:
|
|
Number of Employees
|
|
Type of Job
|
|
2009
|
|
|
2008
|
|
Executives
and managers
|
|
|
201 |
|
|
|
146 |
|
Production
and clerical
|
|
|
424 |
|
|
|
359 |
|
Sales
and marketing
|
|
|
1,491 |
|
|
|
1,261 |
|
Research
and development, technology
|
|
|
38 |
|
|
|
38 |
|
TOTAL:
|
|
|
2,154 |
|
|
|
1,804 |
|
As of
December 31, 2008, we had 1,804 full-time employees. Our 2,154
employees, as of December 31, 2009, includes both 305 full time employees and
1,849 individuals hired on a contract basis through agencies. In
2009, we began hiring certain employees on a contract basis, in order to take
advantage of cost efficiencies.
We do not
have any employment agreements in place with our executive
officers. None of the employees are covered by a collective
bargaining agreement, however, we believe our relationship with employees is
good.
Available
Information
We file
various reports with the SEC, including Annual Reports on Form 10-K, Quarterly
Reports on Form 10-Q and Current Reports on From 8-K, which are available though
the SEC’s electronic data gathering, analysis and retrieval system by accessing
the SEC’s home page (http://www.sec.gov). The documents are also available to be
read or copied at the SEC’s Public Reference Room located at 100 F Street, NE,
Washington, D.C., 20549. Information on the Public Reference Room may be
obtained by calling the SEC at 1-800-SEC-0330.
We also
make available free of charge through our website (www.cski.com.cn) our Annual
Report on Form 10-K, Quarterly Reports on Form 10-Q, Current Reports on Form
8-K, and, if applicable, amendments to those reports filed or furnished pursuant
to the Exchange Act as soon as reasonably practicable after we electronically
file such material with, or furnishes it to, the SEC.
Item
1A. Risk Factors.
We
are subject to certain risks and uncertainties as described
below. These risks and uncertainties may not be the only ones we
face. There may be additional risks that we do not presently know of,
or that we currently consider immaterial. All of these risks could
adversely affect our business, financial condition, results of operations and
cash flows. Our business and operations may be adversely affected if
any of such risks are realized. All investors should consider the
following risk factors before deciding to purchase or sell our
securities.
Risks
Related to Our Business
Adverse
economic conditions may harm our business.
In 2008,
general worldwide economic conditions declined due to sequential effects of the
sub prime lending crisis, general credit market crisis, collateral effects on
the finance and banking industries, concerns about inflation, slower economic
activity, decreased consumer confidence, reduced corporate profits and capital
spending, adverse business conditions and liquidity concerns. This
global economic downturn poses a risk as consumers and businesses may postpone
spending, or seek new ways to eliminate spending, in response to these uncertain
and challenging economic conditions. In addition, there could be a
number of follow-on effects including foreign currency exchange rate
fluctuations, insolvency of key suppliers and customer
insolvencies. We cannot predict the timing or duration of any
economic slowdown or recession or the timing or strength of a subsequent
recovery, worldwide, or in the specific markets we serve. If the
markets for our products significantly deteriorate due to these economic
effects, our business, financial condition and results of operations may be
materially and adversely affected.
Certain
officers and directors have significant control over our company.
Liu
Yan-qing and Han Xiao-yan, who are officers and directors of ours, also serve as
officers and directors of ACPG, TDR and its subsidiaries. As of the
date hereof, Dr. Liu and Ms. Han own, in the aggregate, approximately 36.5% of
the issued and outstanding shares of our common stock. As a result,
these shareholders are effectively able to control certain corporate governance
matters requiring shareholders’ approval. Such matters may include
transactions in which they have an interest other than as a shareholder of ours,
the approval of significant corporate transactions such as increasing the
authorized number of our shares to complete acquisitions or raise capital, if
necessary, and any other transactions requiring a majority vote without seeking
other shareholders’ approval. These persons also have the ability to
control other matters requiring shareholder approval including our election of
directors which could result in the entrenchment of management.
We
depend on our key management personnel and the loss of their services could
adversely affect our business.
We place
substantial reliance upon the efforts and abilities of our executive officers,
Liu Yan-qing, President, Chief Executive Officer and Chairman of the Board, Han
Xiao-yan, Vice Chairman, and Stanley Hao, Chief Financial Officer and
Secretary. We do not have employment agreements with these members of
management. Accordingly, if any of these persons should leave the
company, we would have no remedy or protections in place and would not be able
to prevent them from competing with us or working for
competitors. The loss of the services of any of these executive
officers could have a material adverse effect on our business, operations,
revenues or prospects. In addition, we do not maintain key man life
insurance on the lives of these individuals.
Our
expansion plan may not be successful.
Part of
our strategy is to continue our growth through increasing the distribution and
sales of our products by penetrating existing markets in the PRC, and entering
new geographic markets in the PRC as well as Asia, the United States and other
countries. However, many obstacles to entering such new markets exist,
including, but not limited to, international trade and tariff barriers,
regulatory constraints, product liability concerns, shipping and delivery costs,
costs associated with marketing efforts abroad and maintaining attractive
foreign exchange ratios. Moreover, our expansion strategy may be
based on incorrect assumptions and may be flawed, and may even damage our
performance, competitive position in the market and, ultimately, even our
ability to survive in the marketplace. We cannot, therefore, assure
shareholders that we will be able to successfully overcome such obstacles and
establish our products in any additional markets. Our inability to
implement this growth strategy successfully may have a negative impact on our
growth, future financial condition, results of operations or cash
flows.
There
are many safety risks involved in our products and services that could expose us
to liability or inhibit our ability to secure insurance.
Our
products and services involve direct or indirect impact on human health and
life. The products we manufacture and sell may be flawed and cause
dangerous side effects, and even fatality in certain cases, leading to major
business losses and legal and other liabilities and damages to our
company. In the event that any of our products are alleged to have
adverse side effects, we could be subject to product liability
claims. In addition to the threat of liability, there may be
insurance costs if we enter into certain markets or may not be able to obtain
insurance for certain products in some countries. Some distributors
may refuse to sell our products in certain countries if they perceive such
products to have a high risk or to be uninsurable.
We
do not maintain any insurance and are exposed to all risks of loss, including
resulting from product liability, property loss or damages, or other harm that
we may cause to customers, vendors, suppliers and other third parties, or
securities law claims.
We do not
maintain liability or property insurance coverage or director and officer
insurance coverage and, therefore, we are self-insured for all risks of
loss. Although we seek to reduce potential liability through measures
such as contractual indemnification provisions with distributors and suppliers,
we cannot assure you that such measures will be enforced or
effective. Our policy is to record losses associated with our lack of
insurance coverage at such time as realized loss is incurred. Historically, we
have not had any material losses in connection with our lack of insurance
coverage and are not party to any material pending legal proceedings as of the
date of this report. Management’s intention is to use our working
capital to fund any such losses incurred due to our exposure to inadequate
insurance coverage. Our operating results could be materially and
adversely affected if we were to pay significant damages or incur significant
defense costs in connection with a claim.
We
are highly dependent upon the public perception and quality of our
products. Additionally, anti-corruption measures taken by the
government to correct corruptive practices in the pharmaceutical industry could
adversely affect our sales and reputation.
We are
highly dependent upon consumers’ perception of the safety and quality of our
products as well as similar products distributed by other
companies. Thus, the mere publication of reports asserting that such
products may be harmful could have a material adverse effect on our business,
regardless of whether these reports are scientifically supported.
The PRC
government has recently taken anti-corruption measures to correct corrupt
practices. In the pharmaceutical industry, such practices include,
among other things, acceptance of kickbacks, bribery or other illegal gains or
benefits by the hospitals and medical practitioners from pharmaceutical
distributors in connection with the prescription of a certain
drug. Substantially all of our sales to our ultimate customers are
conducted through third-party distributors. We have no control over
our third-party distributors, who may engage in corrupt practices to promote our
products. While we maintain strict anti-corruption policies
applicable to our internal sales force and third-party distributors, these
policies may not be effective. If any of our third-party distributors
engage in such practices and the government takes enforcement action, our
products may be seized and our own practices, and involvement in the
distributors’ practices may be investigated. If this occurs, our
sales and reputation may be materially and adversely affected.
Our
success will depend on our research and the ability to develop new
products.
Our
growth depends on our ability to consistently discover, develop and
commercialize new products, and find new and improve on existing technologies,
platforms and products. As such, if we fail to make sufficient
investments in research, to be attentive to consumer needs, or fail to focus on
the most advanced technologies, our current and future products could be
surpassed by more effective or advanced products of other
companies.
We
currently rely on third parties to supply the key raw materials we use to
produce our products.
Our
business depends upon the availability of key raw materials. We rely
on only external suppliers for these raw materials. In fiscal year
2009, Harbin Zhong Jia Medicine Company and Heilongjiang Kangda Medicine Company
accounted for approximately 16% and 42% of our total inventory purchases,
respectively. Heilongjiang Kangda Medicine Company accounted for
approximately 33% of our total inventory purchases for the year ended December
31, 2008. For the 2010 fiscal year, we expect that our raw material
suppliers will be substantially similar to last year and the amount of raw
materials will increase commensurate with the increase in the demand of our
products. If any of our major suppliers were to default or become
unable to deliver the raw materials in sufficient quantities, we may be
unable to purchase these raw materials from alternative sources on the same or
similar terms, which could result in a significant decrease in our operating
costs. In addition, any disruption in the supply of our raw materials
could cause delay in the delivery of our products which would be harmful to our
sales reputation and business. If supply is disrupted the increased
amount we have to pay for raw materials could negatively impact our margins,
cause us to cease production if an alternate supplier cannot be
found. If we are unable to procure replacement supplies, our ability
to meet the production demands of our customers could cause the loss of
costumers and/or market share. Our financial results could be
negatively impacted by the lost sales or decreased margins.
We
are dependent on a limited number of customers for a significant portion of our
revenues and accounts receivable and this dependence is likely to
continue.
We have
been dependent on a limited number of customers for a significant portion of our
revenue. For the year ended December 31, 2009, sales to Harbin Shiji
Baolong Medicine Company and Shanxi Xintai Medicine Company accounted for
approximately 16% and 11% of total revenues, respectively. For the
year ended December 31, 2008, sales to Shanxi Xintai and Harbin Shiji Baolong
accounted for 15% and 12% of our total revenues, respectively. For
the year ended December 31, 2007, sales to Ning BoYue Hua Trading Company and
Guang Zhou Xing He Trading Company accounted for approximately 14% and 11% of
our total revenues, respectively. Dependence on a few customers could
make it difficult to negotiate attractive prices for our products and could
expose us to the risk of substantial losses if any such customer stops
purchasing our products. We expect that a limited number of customers
will continue to contribute to a significant portion of our sales in the near
future. Our ability to maintain close relationships with these top customers is
essential to the growth and profitability of our business. If we fail
to sell our products to one or more of these top customers in any particular
period, or if a large customer purchases fewer of our products, defers orders or
fails to place additional orders with us, or if we fail to develop additional
major customers, our revenue would likely decline and our results of operations
would be adversely affected.
In
addition, our accounts receivable are concentrated among a small number of our
customers. Harbin Bao Da Medicine Company and Harbin Shiji Baolong
Medicine Company accounted for approximately 16% and 14% of our accounts
receivable in 2009, respectively. Harbin Shiji Baolong and Shanxi
Xintai accounted for approximately 29% and 11% of our accounts receivable in
2008, respectively. Hua Li Jiu Zhou Company accounted for
approximately 11% of our accounts receivable in 2007. If any our customers fail
to pay us on a timely basis, or do not pay us at all, our business, cash flow,
financial condition and results of operations may be materially and adversely
affected.
Significant
competition from existing and new entities could adversely affect revenues and
profitability.
We
compete with other companies, many of which are developing and/or offering, or
can be expected to develop and offer, products similar to ours. Our
market is a large market with many competitors. Many of our
competitors are more established than we are, and have significantly greater
financial, technical, marketing and other resources than us. Some of
our competitors have greater name recognition and a larger customer
base. These competitors may be able to respond more quickly to new or
changing opportunities and customer requirements and may be able to undertake
more extensive promotional activities, offer more attractive terms to customers,
and adopt more aggressive pricing policies. We cannot assure
investors that we will be able to compete effectively with current or future
competitors or that the competitive pressures we face will not harm our
business.
We
are subject to market and channel risks.
In fiscal
year 2009, over 92% of our sales were made in the PRC, where we primarily sell
our products through drug chain stores. Because of this, we are
dependent to a large degree upon the success of our PRC-based distribution
channel, as well as the success of specific retailers in the distribution
channel. We rely on these distribution channels to purchase, market,
and sell our products. Our success is dependent, to a large degree,
on the growth and success of the drug stores, which may be outside our
control. There can be no assurance that the drug store distribution
channels will be able to grow or prosper as they faces price and service
pressure from other channels, including the mass market. There can be
no assurance that retailers in the drug store distribution channel, in the
aggregate, will respond or continue to respond to our marketing commitment in
these channels.
We
may have difficulty in defending intellectual property rights from
infringement.
Our TCM
products are generally not protected by patents but by trade
secrets. Certain TCM license agreements are made on a non-exclusive
basis. Our success depends, in large part, on our ability to protect
current and future technologies and products and to defend our intellectual
property rights. If we fail to protect our intellectual property
adequately, competitors may manufacture and market similar
products. We have filed patent applications seeking to protect newly
developed and/or technologies. Some patent applications in the PRC
are maintained in secrecy until the patent is issued. Because the
publication of discoveries tends to follow their actual discovery by many
months, we may not be the first to invent, or file patent applications on any of
its discoveries. Patents may not be issued with respect to any of our
patent applications and existing or future patents issued to or licensed by us
may not provide competitive advantages for its products. Patents that
are issued may be challenged, invalidated or circumvented by
competitors. Furthermore, our patent rights may not prevent our
competitors from developing, using or commercializing products that are similar
or functionally equivalent to our products.
To the
extent that we market products in other countries, we may have to take
additional action to protect our intellectual property. The measures
we take to protect our proprietary rights may be inadequate, and we cannot
provide any assurance that our competitors will not independently develop
formulations and processes that are substantially equivalent or superior to our
products or copy our products.
We also
rely on trade secrets, non-patented proprietary expertise and continuing
technological innovation that we seek to protect, in part, by entering into
confidentiality agreements with licensees, suppliers, employees and
consultants. These agreements may be breached and there may not be
adequate remedies in the event of a breach. Disputes may arise
concerning the ownership of intellectual property or the applicability of
confidentiality agreements. Moreover, trade secrets and proprietary
technologies may otherwise become known or be independently developed by
competitors. If patents are not issued with respect to products
arising from research, we may not be able to maintain the confidentiality
of information relating to these products.
We
will be subject to risks relating to third parties that may claim that we
infringe on their proprietary rights and may prevent us from manufacturing and
selling certain of our products.
There has
been substantial litigation in the pharmaceutical and nutraceutical industries
with respect to the manufacturing, use and sale of new
products. These lawsuits relate to the validity and infringement of
patents or proprietary rights of third parties. We may be required to
commence or defend against charges relating to the infringement of patent or
proprietary rights. Any such litigation could involve or result
in:
|
·
|
the
incurrence of substantial expense, even if we are successful in the
litigation;
|
|
·
|
a
diversion of significant time and effort of technical and management
personnel;
|
|
·
|
the
loss of our rights to develop or make certain products;
and
|
|
·
|
the
payment of substantial monetary damages or royalties in order to license
proprietary rights from third
parties.
|
Although
patent and intellectual property disputes within these industries have often
been settled through licensing or similar arrangements, costs associated with
these arrangements may be substantial and could include the long-term payment of
royalties. These arrangements may be investigated by regulatory
agencies and, if improper, may be invalidated. Also, the required
licenses may not be made available to us on acceptable
terms. Accordingly, an adverse determination in a judicial or
administrative proceeding or a failure to obtain necessary licenses could
prevent our company from manufacturing and selling some of our products or
increase costs to market these products.
In
addition, when seeking regulatory approval for some of our products, we are
required to certify to regulatory authorities, including the SFDA that such
products do not infringe upon third party patent rights. Filing a
certification against a patent gives the patent holder the right to bring a
patent infringement lawsuit against us. Any lawsuit would delay
regulatory approval by the SFDA. A claim of infringement and the
resulting delay could result in substantial expenses and even prevent us from
manufacturing and selling certain of our products.
The
launch of a product prior to a final court decision or the expiration of a
patent held by a third party may result in substantial damages to
us. Depending upon the circumstances, a court may award the patent
holder damages equal to three times their loss of income. If we
are found to infringe a patent held by a third party and become subject to such
treble damages, these damages could have a material adverse effect on our
results of operations and financial condition.
Our
failure to comply with accounting policies and regulations in making reasonable
estimates and judgments could negatively impact our financial position and
results of operation.
We are
subject to critical accounting policies and actual results may vary from
estimates. We have followed, and will continue to follow, generally
accepted accounting principles for the United States in preparing financial
statements. As part of this work, we must make many estimates and
judgments concerning future events. These affect the value of the
assets and liabilities, contingent assets and liabilities, and revenue and
expenses reported in such financial statements. We believe that
these estimates and judgments are reasonable, and we have made them in
accordance with accounting policies based on information available at the
time. However, actual results could differ from estimates, and this
could require us to record adjustments to expenses or revenues that could be
material to our financial position and results of operations in the
future.
Our
business is subject to many governmental regulatory and policy
risks.
Our
business must be conducted in compliance with various government regulations and
in particular, the SFDA’s regulations. Government regulations may
have material impact on our operations, increase costs and could prevent or
delay the manufacturing and selling of our products. Research,
development, testing, manufacturing and marketing activities are subject to
various governmental regulations in China, including health and drug
regulations. Government regulations, among other things, cover the
inspection of and controls over testing, manufacturing, safety and environmental
considerations, efficacy, labeling, advertising, promotion, record keeping and
sale and distribution of pharmaceutical products. We will not be able
to license, manufacture, sell and distribute the vast majority of our products
without a proper approval from government agencies and in particular the
SFDA. This approval process is lengthy, with approvals for TCM
products typically occurring 18-24 months after the application is initially
filed. There is no assurance that we will obtain such approvals on a
timely basis, or at all. Delays in obtaining approvals will delay our
ability to market products and denial of approval for a specific product will
result in our inability to market the product and recoup the expenses incurred
in that products development and testing.
In
addition, delays or rejections may be encountered based upon additional
government regulation from future legislation, administrative action or changes
in governmental policy and interpretation during the period of product
development and product assessment. Although we have, so far,
obtained the rights to sell our products in the PRC, we may not continue to
receive and maintain regulatory approvals for the sales of these
products. Our marketing activities are also subject to government
regulations with respect to the prices that it intends to charge or any other
marketing and promotional related activities. Government regulations
may substantially increase the costs for developing, licensing, manufacturing
and selling products, impacting negatively our operations, revenue, income and
cash flow.
There
could be changes in government regulations towards the pharmaceutical and
nutraceutical industries that may adversely affect our business.
The
manufacture and sale of pharmaceutical and nutraceutical products in the PRC is
heavily regulated by many state, provincial and local
authorities. These regulations significantly increased the difficulty
and costs involved in obtaining and maintaining regulatory approvals for
marketing new and existing products. Our future growth and
profitability depends to a large extent on our ability to obtain regulatory
approvals.
The SFDA
has implemented new guidelines for licensing of pharmaceutical
products. All existing manufacturers with licenses, which are
currently valid under the previous guidelines, were required to apply for the
GMP certifications by June 30, 2004, and to receive approvals by December 31,
2004. We received certifications for our current
products. However, should we fail to maintain the GMP certifications
under the new guidelines in the future, or for new products, our businesses
would be materially and adversely affected.
Moreover,
the laws and regulations regarding acquisitions of the pharmaceutical and
nutraceutical industries in the PRC may also change and may significantly impact
our ability to grow through acquisitions.
We
need to manage growth in operations to maximize our potential growth and achieve
our expected revenues.
Our
success depends on our ability to achieve continued growth. In order
to maximize potential growth in current and potential markets, we believe that
we must expand our manufacturing and marketing operations. This
expansion will place a significant strain on management and operational,
accounting and information systems and will require substantial additional
capital. We will need to continue to improve financial controls,
operating procedures, and management information systems if and as we
grow. We will also need to effectively train, motivate, and manage
our employees. A failure to manage our growth could disrupt
operations and ultimately prevent us from generating the revenues we
expect.
International
operations require our company to comply with a number of U.S. and international
regulations.
We are
required to comply with a number of international regulations in countries
outside of the United States. In addition, we must comply with the
Foreign Corrupt Practices Act, or FCPA, which prohibits U.S. companies or their
agents and employees from providing anything of value to a foreign official for
the purposes of influencing any act or decision of these individuals in their
official capacity to help obtain or retain business, direct business to any
person or corporate entity or obtain any unfair advantage. Any
failure to adopt appropriate compliance procedures and ensure that our employees
and agents comply with the FCPA and applicable laws and regulations in
foreign jurisdictions could result in substantial penalties and/or restrictions
in our ability to conduct business in certain foreign
jurisdictions. The U.S. Department of The Treasury’s Office of
Foreign Asset Control, or OFAC, administers and enforces economic and trade
sanctions against targeted foreign countries, entities and individuals based on
U.S. foreign policy and national security goals. As a result, we are
restricted from entering into transactions with certain targeted foreign
countries, entities and individuals except as permitted by OFAC which may reduce
our future growth.
We
may incur significant costs to ensure compliance with U.S. corporate governance
and accounting requirements.
We are a
public reporting company, and, as such, we will incur significant costs
associated with public company reporting requirements, costs associated with
newly applicable corporate governance requirements, including requirements under
the Sarbanes-Oxley Act of 2002 and other rules implemented by the U.S.
Securities and Exchange Commission (“SEC”). All of these applicable rules and
regulations can be expected to increase legal and financial compliance costs and
to make some activities more time consuming and costly. Management
also expects that these applicable rules and regulations may make it more
difficult and more expensive to obtain director and officer liability insurance
and we may be required to accept reduced policy limits and coverage or incur
substantially higher costs to obtain the same or similar coverage. As
a result, it may be more difficult for us to attract and retain qualified
individuals to serve on our board of directors or as executive
officers.
We
may have difficulty raising necessary capital to fund operations as a result of
market price volatility for our shares of common stock.
In recent
years, the securities markets in the U.S. have experienced a high level of price
and volume volatility, and the market price of securities of many companies have
experienced wide fluctuations that have not necessarily been related to the
operations, performances, underlying asset values or prospects of such
companies. For these reasons, our shares of common stock can also be
expected to be subject to volatility resulting from purely market forces over
which we will have no control. If our business development plans are
successful, we may require additional financing to continue to develop and
exploit existing and new technologies and to expand into new
markets. The exploitation of existing and new technologies may,
therefore, be dependent upon our ability to obtain financing through debt and
equity or other means.
We
are obligated to indemnify our officers and directors for certain losses they
suffer.
To the
fullest extent permitted by Chapter 78 of the Nevada Revised Statues, we may, if
and to the extent authorized by our board of directors, indemnify our officers
and any other persons who we have power to indemnify against liability,
reasonable expense or other matter whatsoever. If we are required to
indemnify any persons under this policy, we may have to pay indemnity in a
substantial amount which we may be unable to recover at all.
Risks
Related to Doing Business in China
Our
business will be affected by the government regulation and Chinese economic
environment because most of our sales will be in the China market.
In 2009,
2008, and 2007, approximately 92%, 92% and 75% of our total revenues,
respectively, were from sales in the PRC. The manufacture and sale of
pharmaceutical products in China is heavily regulated by many state, provincial
and local authorities. The SFDA requires pharmaceutical manufacturers
to obtain GMP certifications. We currently have the certifications
needed for our current operations. However, should we fail to receive
or maintain the GMP certifications in the future, we would no longer be able to
manufacture pharmaceuticals in China, and our businesses would be materially and
adversely affected. These regulations significantly increase the
difficulty and costs involved in obtaining and maintaining regulatory approvals
for marketing new and existing products. Our future growth and
profitability depend to a large extent on our ability to obtain regulatory
approvals. Additionally, the law could change so as to prohibit the
use of certain pharmaceuticals. If one of our products becomes
prohibited, this change would cease the productivity of that
product. The China National Development and Reform Commission
(“CNDRC”), has recently implemented price adjustments on many marketed
pharmaceutical products. We have no control over such governmental
policies, which may impact the pricing and profitability of our
products.
Although
we have started exporting products to other countries, most of our sales are in
the PRC. It is anticipated that our products in the PRC will continue
to represent a significant portion of sales in the near future. As a
result of our reliance on the PRC markets, our operating results and financial
performance could be affected by any adverse changes in economic, political
and social conditions in the PRC.
The
modernization of regulations for the pharmaceutical industry is relatively new
in the PRC, and the manner and extent to which it is regulated will continue to
evolve. As a pharmaceutical company, we are subject to the
Pharmaceutical Administrative Law, which governs the licensing, manufacture,
marketing and distribution of pharmaceutical products in the PRC, and sets
penalty provisions for violations of provisions of the Pharmaceutical
Administrative Law. In addition as a “Foreign Owned
Enterprise,” we will be subject to the Foreign Company provisions of the Company
Law of the PRC. Changes in these laws or new interpretations of
existing laws may have a significant impact on our methods and our cost of
doing business. For example, if legislative proposals for
pharmaceutical product pricing, reimbursement levels, approval criteria or
manufacturing requirements should be proposed and adopted, such new legislation
or regulatory requirements may have a material adverse effect on our financial
condition, results of operations or cash flows. In addition, we are
subject to varying degrees of regulation and licensing by governmental agencies
in China. At this time, we are unaware of any China legislative proposals that
could adversely affect our business. There can be no assurance that future
regulatory, judicial and legislative changes will not have a material adverse
effect on our operations, that regulators or third parties will not raise
material issues with regard to compliance or non-compliance with applicable laws
or regulations, or that any changes in applicable laws or regulations will not
have a material adverse effect on our business.
Certain
political and economic considerations relating to China could adversely affect
us.
China is
transitioning from a planned economy to a market economy. While the
PRC government has pursued economic reforms since its adoption of the open-door
policy in 1978, a large portion of the Chinese economy is still operating under
five-year plans and annual state plans. Through these plans and other
economic measures, such as control on foreign exchange, taxation and
restrictions on foreign participation in the domestic market of various
industries, the PRC government exerts considerable direct and indirect influence
on the economy. Many of the economic reforms carried out by the PRC
government are unprecedented or experimental, and are expected to be refined and
improved. Other political, economic and social factors can also lead
to further readjustment of such reforms. This refining and
readjustment process may not necessarily have a positive effect on our
operations or future business development. Our operating results may
be adversely affected by changes in China’s economic and social conditions as
well as by changes in the policies of the PRC government, such as changes in
laws and regulations, or the official interpretation thereof, which may be
introduced to control inflation, changes in the interest rate or method of
taxation, and the imposition of additional restrictions on currency
conversion.
Accordingly,
government actions in the future, including any decision not to continue to
support recent economic reforms and to return to a more centrally planned
economy or regional or local variations in the implementation of economic
policies, could have a significant effect on economic conditions in China or
particular regions thereof, and could require us to divest ourselves of any
interest we then hold in Chinese properties or joint ventures.
There
are risks inherent in doing business in China.
The PRC
is a developing country with a young market economic system overshadowed by the
state under heavy regulation and scrutiny. Its political and economic
systems are very different from the more developed countries. China
also faces many social, economic and political challenges that may produce major
shocks and instabilities and even crises, in both its domestic arena and in its
relationship with other countries, including but not limited to the United
States. Such shocks, instabilities and crises may in turn
significantly and adversely affect our performance.
The
recent nature and uncertain application of many PRC laws applicable to our
company create an uncertain environment for business operations and they could
have a negative effect on our business and operations.
The PRC
legal system is a civil law system. Unlike the common law system, the
civil law system is based on written statutes in which decided legal cases have
little value as precedents. In 1979, the PRC began to promulgate a
comprehensive system of laws and has since introduced many laws and regulations
to provide general guidance on economic and business practices in the PRC and to
regulate foreign investment. Progress has been made in the
promulgation of laws and regulations dealing with economic matters such as
corporate organization and governance, foreign investment, commerce, taxation
and trade. However, there are substantial uncertainties regarding the
interpretation and application of PRC laws and regulations, including, but not
limited to, the laws and regulations governing our business. In addition, the
effectiveness of newly-enacted laws, regulations or amendments may be
delayed, resulting in detrimental reliance by investors. New laws and
regulations that affect existing and proposed future businesses may also be
applied retroactively. The promulgation of new laws, changes of existing laws
and the abrogation of local regulations by national laws could have a negative
impact on our business, business prospects and operations. In
addition, as these laws, regulations and legal requirements are relatively
recent, their interpretation and enforcement involve significant
uncertainty.
Our
business may be affected by unexpected changes in regulatory requirements in the
jurisdictions in which we operate.
Our
company, and its subsidiaries, are subject to many general regulations governing
business entities and their behavior in China and in other jurisdictions in
which we and our subsidiaries have, or plan to have, operations and market
products. In particular, we are subject to laws and regulations
covering food, dietary supplements and pharmaceutical
products. Such regulations typically deal with licensing,
approvals and permits. Any change in product licensing may make our
products more or less available on the market. Such changes may have
a positive or negative impact on the sale of our products and may directly
impact the associated costs in compliance and our operational and financial
viability. Such regulatory environment also covers any existing or
potential trade barriers in the form of import tariff and taxes that may make it
difficult for us to import our products to certain countries and regions, such
as Hong Kong, which would limit its international expansion.
A
slowdown or other adverse developments in the PRC economy may materially and
adversely affect our customers, demand for our services and our
business.
All of
our operations are conducted in the PRC and almost all of our revenues are
generated from sales in the PRC. Although the PRC economy has grown
significantly in recent years, we cannot assure you that such growth will
continue. According to the PRC National Bureau of Statistics, the
PRC’s economy expended 6.8% from a year earlier in the fourth quarter of 2008,
which means that a full-year growth for 2008 was 9.0%. It is the
first time since 2002 that the PRC has expanded by less than 10%
annually. A number of factors have contributed to this slow-down,
including appreciation of the RMB, which has adversely affected the PRC’s
exports. In addition, the slow-down has been exacerbated by the recent global
crisis in the financial services and credit markets, which has resulted in
significant volatility and dislocation in the global capital markets. It is
uncertain how long the global crisis in the financial services and credit
markets will continue and how much adverse impact it will have on the global
economy in general or the PRC economy in particular. We do not know
how sensitive we are to a slowdown in economic growth or other adverse changes
in the PRC economy which may affect demand for our products. A
slowdown in overall economic growth, an economic downturn or recession or other
adverse economic developments in the PRC may materially reduce the demand for
our products and materially and adversely affect our business.
Inflation
in the PRC could negatively affect our profitability and growth.
While the
PRC economy has experienced rapid growth, it has been uneven among various
sectors of the economy and in different geographical areas of the country. Rapid
economic growth can lead to growth in the money supply and rising inflation. If
prices for our products do not rise at a rate that is sufficient to fully
absorb inflation-driven increases in our costs of supplies, our profitability
can be adversely affected.
During
the past ten years, the rate of inflation in the PRC has been as high as 20.7%
and as low as 2.2%. These factors have led to the adoption by the Chinese
government, from time to time, of various corrective measures designed to
restrict the availability of credit or regulate growth and contain inflation. In
order to control inflation in the past, the PRC government has imposed controls
on bank credits, limits on loans for fixed assets and restrictions on state bank
lending. The implementation of these and other similar policies can impede
economic growth and thereby harm the market for our products.
Substantially
all of our assets are located in the PRC and all of our revenues are derived
from our operations in the PRC. Accordingly, our results of
operations and prospects are subject, to a significant extent, to the economic,
political and legal developments in the PRC.
Substantially
all of our assets are located in the PRC and all of our revenues are derived
from our operations in the PRC. Accordingly, our results of
operations and prospects are subject, to a significant extent, on the economic,
political and legal developments in the PRC. The PRC economy differs
from the economies of most developed countries in many respects.
Since
1978, the PRC has been one of the world’s fastest-growing economies in terms of
gross domestic product, or GDP growth. We cannot assure you, however, that such
growth will be sustained in the future. If, in the future, the PRC’s economy
experiences a downturn or grows at a slower rate than expected, there may be
less demand for spending in certain industries.
Our
ability to implement our business plan is based on the assumption that the
Chinese economy will continue to grow. The PRC’s economic growth has been
uneven, both geographically and among various sectors of the economy. The PRC
government has implemented various measures to encourage economic growth and
guide the allocation of resources. Some of these measures benefit the overall
PRC economy, but may also have a negative effect on us.
The PRC
economy has been transitioning from a planned economy to a more market-oriented
economy. Although in recent years the PRC government has implemented measures
emphasizing the use of market forces for economic reform, the reduction of state
ownership of productive assets and the establishment of sound corporate
governance in business enterprises, a substantial portion of productive assets
in the PRC is still owned by the PRC government. In addition, the PRC government
continues to play a significant role in regulating industry development by
imposing industrial policies. It also exercises significant control over PRC
economic growth through the allocation of resources, controlling payment of
foreign currency-denominated obligations, setting monetary policy and providing
preferential treatment to particular industries or companies. We cannot assure
you that changes in the PRC’s economic, political or legal systems will not
detrimentally affect our business, prospects, financial conditions and results
of operations.
We
may have difficulty attracting talent in foreign countries.
Currently,
over 92% of our sales are in the PRC. We are in the process of
attempting to establish marketing and sales presence in the U.S. and other
countries. We expect to establish an office in the U.S. for investor
relations. In the future, we may explore expanding its operations in
other countries throughout the world. Upon effecting any such
expansion, we may not be able to identify and retain qualified personnel due to
its lack of understanding of different cultures and lack of local
contacts. This may impede international expansion.
Currency
conversion and exchange rate volatility could adversely affect our financial
condition, by making acquisitions in China or of Chinese products more
expensive.
The PRC
government imposes control over the conversion of Renminbi (“RMB”), the currency
of China, into foreign currencies. Under the current unified floating
exchange rate system, the People’s Bank of China publishes an exchange rate,
referred to as the PBOC exchange rate, based on the previous day’s dealings
in the inter-bank foreign exchange market. Financial institutions
authorized to deal in foreign currency may enter into foreign exchange
transactions at exchange rates within an authorized range above or below the
PBOC exchange rate according to market conditions.
Pursuant
to the Foreign Exchange Control Regulations of the PRC issued by the State
Council which came into effect on April 1, 1996, and the Regulations on the
Administration of Foreign Exchange Settlement, Sale and Payment of the PRC which
came into effect on July 1, 1996, regarding foreign exchange control, conversion
of RMB into foreign exchange by Foreign Investment Enterprises (“FIEs”), for use
on current account items, including the distribution of dividends and profits to
foreign investors, is permissible. FIEs are permitted to convert
their after-tax dividends and profits to foreign exchange and remit such foreign
exchange to their foreign exchange bank accounts in the PRC.
Conversion
of RMB into foreign currencies for capital account items, including direct
investment, loans, and security investment, is still subject to certain
restrictions. On January 14, 1997, the State Council amended the
Foreign Exchange Control Regulations and added, among other things, an important
provision, which provides that the PRC government shall not impose restrictions
on recurring international payments and transfers under current account
items. These rules are subject to change.
Enterprises
in the PRC (including FIEs) which require foreign exchange for transactions
relating to current account items, may, without approval of the State
Administration of Foreign Exchange (“SAFE”) effect payment from their foreign
exchange account or convert and pay at the designated foreign exchange banks by
providing valid receipts and proofs.
Convertibility
of foreign exchange in respect of capital account items, such as direct
investment and capital contribution, is still subject to certain restrictions,
and prior approval from the SAFE or its relevant branches must be
sought.
Our
company is a FIE to which the Foreign Exchange Control Regulations are
applicable. There can be no assurance that we will be able to obtain
sufficient foreign exchange to pay dividends or satisfy other foreign exchange
requirements in the future.
Since
1994, the exchange rate for RMB against the U.S. dollar has remained relatively
stable, most of the time in the region of approximately RMB 8.00 to
U.S.$1.00. However, in 2005, the Chinese government announced that
would begin pegging the exchange rate of the Chinese RMB against a number of
currencies, rather than just the U.S. dollar. Currently, exchange
rates are approximately RMB 6.84 to U.S.$1.00 resulting in the increase in price
of Chinese products to U.S. purchasers. As our operations are
primarily in China, any significant revaluation of the Chinese RMB may
materially and adversely affect cash flows, revenues and financial
condition. For example, to the extent that we need to convert United
States dollars into Chinese RMB for operations, appreciation of this currency
against the U.S. dollar could have a material adverse effect on our business,
financial condition and results of operations. Conversely, if we
decide to convert Chinese RMB into U.S. dollars for other business purposes and
the U.S. dollar appreciates against this currency, the U.S. dollar equivalent of
the Chinese RMB that we convert would be reduced.
Restrictions
on currency exchange may limit our ability to utilize our revenues effectively
and the ability of the PRC entities to obtain financing.
Substantially
all of our revenues and operating expenses are denominated in Renminbi.
Restrictions on currency exchange imposed by the PRC government may limit our
ability to utilize revenues generated in Renminbi to fund our business
activities outside the PRC, if any, or expenditures denominated in foreign
currencies. Under current PRC regulations, Renminbi may be freely converted into
foreign currency for payments relating to “current account transactions,” which
include among other things dividend payments and payments for the import of
goods and services, by complying with certain procedural requirements. The PRC
entities may also retain foreign exchange in their respective current account
bank accounts, subject to a cap set by the State Administration for Foreign
Exchange, or SAFE, or its local counterpart, for use in payment of international
current account transactions. However, conversion of Renminbi into foreign
currencies, and of foreign currencies into Renminbi, for payments relating
to “capital account transactions,” which principally includes investments
and loans, generally requires the approval of SAFE and other relevant PRC
governmental authorities. Restrictions on the convertibility of the Renminbi for
capital account transactions could affect the ability of the PRC entities to
make investments overseas or to obtain foreign exchange through debt or equity
financing, including by means of loans or capital contributions from the parent
entity.
Any
existing and future restrictions on currency exchange may affect the ability of
the PRC entities or an affiliated entity to obtain foreign currencies, limit our
ability to utilize revenues generated in Renminbi to fund any business
activities outside the PRC that are denominated in foreign currencies, or
otherwise materially and adversely affect our business.
We
are required to be in compliance with the registered capital requirements of the
PRC.
Under the
Company Law of the PRC, we are required to contribute a certain amount
of “registered capital” to our wholly owned subsidiary. By
law, our subsidiaries are required to contribute at least 10% of after tax net
income (as determined in accordance with Chinese GAAP) into a statutory surplus
reserve until the reserve is equal to 50% of our and our subsidiaries’
registered capital, and between 5% and 10% of its after tax net income, as
determined by our board of directors, into a public welfare
fund. These reserve funds are recorded as part of shareholders’
equity but are not available for distribution to shareholders other than in the
case of liquidation. As a result of this requirement, the amount of
net income available for distribution to shareholders will be
limited.
Dividends
we receive from our subsidiaries located in the PRC may be subject to PRC
withholding tax.
The PRC’s
Enterprise Income Tax Law (“EIT Law”) provides that an income tax rate of 10%
may be applicable to dividends payable to non-PRC investors that are
“non-resident enterprises.” Non-resident enterprises refer to enterprises which
do not have an establishment or place of business in the PRC, or which have such
establishment or place of business in the PRC but the relevant income is not
effectively connected with the establishment or place of business, to the extent
such dividends are derived from sources within the PRC. The income tax for the
non-resident enterprises shall be subject to withholding at income source with
the payer acting as the obligatory withholder under the EIT Law, and therefore,
such income tax is generally called “withholding tax” in practice. It
is currently unclear in what circumstances a source will be considered as
located within the PRC. As a U.S. holding company and substantially
all of our income will be derived from dividends we receive from our PRC
operating subsidiaries. Thus, if we are considered as a “non-resident
enterprise” under the EIT Law and the dividends paid to us by our PRC operating
subsidiaries are considered income sourced within the PRC, such dividends may be
subject to a 10% withholding tax. No dividends were paid to us by our
PRC operating subsidiaries in 2007, 2008 or 2009.
Deterioration
of the PRC’s political relations with the U.S., Europe, or other nations could
make Chinese businesses less attractive to Western investors.
The
relationship between the U.S. and the PRC is subject to sudden fluctuation and
periodic tension. Changes in political conditions in the PRC and changes in the
state of Sino-foreign relations are difficult to predict and could materially
adversely affect our operations or cause potential target businesses or services
to become less attractive. This could lead to a decline in our profitability.
Any weakening of relations between the U.S., Europe, or other nations and the
PRC could have a material adverse effect on our operations or our ability
to raise additional capital.
The
discontinuation of any of the preferential tax treatments currently available to
the PRC entities could materially increase our tax liabilities.
The rate
of income tax on companies in China may vary depending on the availability of
preferential tax treatment or subsidies based on their industry or location. The
current maximum corporate income tax rate is 33%. The new Enterprise Income Tax
Law became effective as of January 1, 2008, pursuant to which, an enterprise
income tax of 25% applies to any enterprise. Although we were approved by the
local tax authority to be exempted from the enterprise income tax for a
five-year period commencing in 2007 and ending in 2012, we do not know whether
such new law will change the preferential treatment that was granted to us. Any
loss or substantial reduction of the tax benefits enjoyed by us would reduce our
net profit.
Because
PRC law governs almost all of our operating subsidiaries’ material agreements,
we may not be able to enforce our rights within the PRC or elsewhere, which
could result in a significant loss of business, business opportunities or
capital.
PRC law
governs almost all of the material agreements of our subsidiaries. We cannot
assure you that we will be able to enforce any of our material agreements or
that remedies will be available outside of the PRC. The Chinese legal
system is similar to a civil law system based on written statutes. Unlike common
law systems, it is a system in which decided legal cases have little
precedential value. In 1979, the PRC government began to promulgate a
comprehensive system of laws and regulations governing economic matters in
general. The overall effect of legislation since then has been to
significantly enhance the protections afforded to various forms of foreign
investment in the PRC. Certain of our subsidiaries are wholly
foreign-owned enterprises, and are subject to laws and regulations applicable to
foreign investment in the PRC in general and laws and regulations applicable to
wholly foreign-owned enterprises in particular. Relevant PRC laws,
regulations and legal requirements may change frequently, and their
interpretation and enforcement involve uncertainties. For example, we
may have to resort to administrative and court proceedings to enforce the
legal protection that we enjoy either by law or contract. However, since PRC
administrative and court authorities have significant discretion in interpreting
and implementing statutory and contractual terms, it may be more difficult to
evaluate the outcome of administrative and court proceedings and the level of
legal protection we enjoy than under more developed legal
systems. Such uncertainties, including the inability to enforce our
contracts, could materially and adversely affect our business and
operations. In addition, confidentiality protections in the PRC may
not be as effective as in the U.S. or other countries. Accordingly,
we cannot predict the effect of future developments in the PRC legal system,
particularly with respect to financing sectors, including the promulgation of
new laws, changes to existing laws or the interpretation or enforcement thereof,
or the preemption of local regulations by national laws. These
uncertainties could limit the legal protections available to us and other
foreign investors.
Our
PRC subsidiaries are obligated to withhold and pay PRC individual income tax on
behalf of our employees who are subject to PRC individual income tax. If we fail
to withhold or pay such individual income tax in accordance with applicable PRC
regulations, we may be subject to certain sanctions and other penalties and may
become subject to liability under PRC laws.
Under PRC
laws, our PRC subsidiaries are obligated to withhold and pay individual income
tax on behalf of our employees who are subject to PRC individual income tax. If
we fail to withhold and/or pay such individual income tax in accordance with PRC
laws, we may be subject to certain sanctions and other penalties and may become
subject to liability under PRC laws.
In
addition, the State Administration of Taxation has issued several circulars
concerning employee stock options. Under these circulars, our employees working
in the PRC (which could include both PRC employees and expatriate employees
subject to PRC individual income tax) who exercise stock options will be subject
to PRC individual income tax. Our PRC subsidiaries have obligations to file
documents related to employee stock options with relevant tax authorities and
withhold and pay individual income taxes for those employees who exercise their
stock options. While tax authorities may advise us that our policy is compliant,
they may change their policy, and we could be subject to sanctions.
Failure
to comply with the U.S. Foreign Corrupt Practices Act could subject us to
penalties and other adverse consequences.
We are
required to comply with the U.S. Foreign Corrupt Practices Act, which generally
prohibits U.S. companies from engaging in bribery or other prohibited payments
to foreign officials for the purpose of obtaining or retaining business. Foreign
companies, including some that may compete with us, are not subject to these
prohibitions, and therefore may have a competitive advantage over us.
Corruption, extortion, bribery, pay-offs, theft and other fraudulent practices
may occur in the PRC. If our competitors engage in these practices
they may receive preferential treatment, giving our competitors an advantage in
securing business, which would put us at a disadvantage. We can make no
assurance that our employees or other agents will not engage in such conduct for
which we might be held responsible. If our employees or other agents are found
to have engaged in such practices, we could suffer severe penalties and other
consequences that may have a material adverse effect on our business, financial
condition and results of operations.
We
face risks related to health epidemics and outbreak of contagious
disease.
Our
business could be materially and adversely affected by the effects of H1N1 Flu,
Avian Flu, Severe Acute Respiratory Syndrome (“SARS”) or other epidemics or
outbreaks. In April 2009, an outbreak of H1N1 Flu first occurred in
Mexico and quickly spread to other countries, including the U.S. and the PRC.
In the last decade, the PRC has suffered health epidemics related to the
outbreak of Avian Flu and SARS. Any prolonged occurrence or
recurrence of H1N1 Flu , Avian Flu, SARS or other adverse public health
developments in the PRC may have a material adverse effect on our business and
operations. These health epidemics could result in severe travel
restrictions and closures that would restrict our ability to ship our
products. Potential outbreaks could also lead to temporary closure of
our manufacturing facilities, our suppliers’ facilities and/or our end-user
customers’ facilities, leading to reduced production, delayed or cancelled
orders, and decrease in demand for our products. Any future health epidemic or
outbreaks that could disrupt our operations and/or restrict our shipping
abilities may have a material adverse effect on our business and results of
operations.
Risks
Relating to the Market for Our Common Stock and our Capital
Structure
Application
of guidance related to the Accounting for Derivative Financial Instruments
Indexed to, and Potentially Settled in, a Company's Own Stock has negatively
impacted our statement of operations for the year ended December 31,
2009 (restated) and could continue to negatively impact our statement of
operations.
For
the year ended December 31, 2009 (restated), we reported an unrealized loss on
derivatives in the consolidated statements of operations of $4,807,000 as a
result of the issuance of warrants to purchase up to an aggregate of 750,000
shares of common stock in our January 2008 private placement. Our
comprehensive income will continue to fluctuate as a result of the impact of
such warrants and will be adversely effected in each reporting period in which
the fair value of the warrants that remain outstanding continue to
increase.
Our
stock price is likely to be highly volatile.
The
trading price of our common stock has been highly volatile. Failure
to meet market expectations in our financial results could cause our stock price
to decline. Moreover, factors that are not related to our operating
performance could cause our stock price to decline. The stock market
has recently experienced significant price and volume fluctuations that have
affected the market prices for securities of technology and communications
companies. Consequently, you may experience a decrease in the market
value of your common stock, regardless of our operating performance or
prospects.
We
do not plan to declare or pay any dividends to our shareholders in the near
future and would need regulatory approval to do so.
We have
not declared any dividends in the past, and we do not intend to distribute
dividends in the near future. The declaration, payment and amount of
any future dividends will be made at the discretion of the board of directors
and subject to PRC law, and will depend upon, among other things, the results of
operations, cash flows and financial condition, operating and capital
requirements, and other factors as the board of directors considers
relevant. There is no assurance that future dividends will be paid,
and if dividends are paid, there is no assurance with respect to the amount of
any such dividend.
We
have the right to issue up to 5,000,000 shares of "blank check"
preferred stock, which may adversely affect the voting power of the holders of
other of our securities and may deter hostile takeovers or delay changes in
management control.
Our
articles of incorporation provides that we may issue up to 5,000,000 shares of
preferred stock from time to time in one or more series, and with such rights,
preferences and designations as our board of directors may determinate from time
to time. Our board of directors, without further approval of our
common stockholders, is authorized to fix the dividend rights and terms,
conversion rights, voting rights, redemption rights, liquidation preferences and
other rights and restrictions relating to any series of our preferred stock.
Issuances of shares of preferred stock could, among other things, adversely
affect the voting power of the holders of other of our securities and may, under
certain circumstances, have the effect of deterring hostile takeovers or
delaying changes in management control. Such an issuance would dilute
existing stockholders, and the securities issued could have rights, preferences
and designations superior to our common stock.
Sales
of our common stock may have an adverse effect on the market price of our common
stock. Additionally, we may issue shares upon exercise of outstanding
warrants that are exercisable at prices that are below current market prices
which will be dilutive to the common stock.
As of
March 15, 2010, we had 16,790,851 shares of common stock outstanding, many of
which are freely transferable under Rule 144. The sale of these
shares may have an adverse effect on the market price for our common
stock.
In
addition, as of March 15, 2010, we had issued and outstanding warrants to
purchase an aggregate of 593,800 shares of our common stock, which are
exercisable at a price of $12.50 per share. Our issuance of
additional shares of common stock upon exercise of our outstanding warrants will
reduce the percentage equity ownership of holders of shares of our common stock.
Further, the exercise of a significant number of warrants, and subsequent
sale of shares of common stock received upon such exercise, could cause a
sharp decline in the market price of our common stock.
FORWARD-LOOKING
STATEMENTS
Some of
the statements contained in this report are not statements of historical or
current fact. As such, they are "forward-looking statements" based on
our current expectations, which are subject to known and unknown risks,
uncertainties and assumptions. They include statements relating
to:
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future
sales and financings;
|
|
·
|
the
future development of our business;
|
|
·
|
our
ability to execute our business
strategy;
|
|
·
|
projected
expenditures; and
|
|
·
|
the
market for our products.
|
You can
identify forward-looking statements by terminology such as "may," "will,"
"should," "could," "expects," "intends," "plans," "anticipates," "believes,"
"estimates," "predicts," "potential" or "continue" or the negative of these
terms or other comparable terminology. These statements are not
predictions. Actual events or results may differ materially from
those suggested by these forward-looking statements. In evaluating
these statements and our prospects generally, you should carefully consider the
factors set forth below. All forward-looking statements attributable
to us or persons acting on our behalf are expressly qualified in their entirety
by these cautionary factors and to others contained throughout this
prospectus. We are under no duty to update any of the forward-looking
statements after the date of this prospectus or to conform these statements to
actual results.
Although
it is not possible to create a comprehensive list of all factors that may cause
actual results to differ from the results expressed or implied by our
forward-looking statements or that may affect our future results, some of these
factors are set forth under "Risk Factors" in this report.
Item.
1B. Unresolved Staff Comments.
None.
Item
2. Properties.
Under
Chinese law, the government owns all of the land in the PRC and companies and
individuals are authorized to use the land only through land use rights granted
by the PRC government.
Our
manufacturing facilities are located in the cities of Harbin and Peng Lai in the
PRC. These facilities are operated in accordance with
GMP. We own these facilities and are not subject to costs associated
under rental or lease obligations.
In
January 2010, we completed the construction of two office buildings and TDR and
Haina moved into these new facilities, located in Song Bei District of Harbin
City, Heilongjiang Province, PRC. It is anticipated that residual
work, including road construction, fire control equipment, amenity
improvement, and final acceptance, will be completed on these facilities in the
third quarter of 2010, at an additional cost of approximately $3.0 million.
We own these facilities and are not subject to costs associated under rental or
lease obligations.
A
breakdown of our facilities by subsidiary is as follows:
|
|
Subsidiaries Facilities as of March 15, 2010, in Square Meters
|
|
|
|
TDR
|
|
|
First
|
|
|
Tianlong
|
|
|
Peng Lai
|
|
Land
Area
|
|
|
35,000 |
|
|
|
40,000 |
|
|
|
15,000 |
|
|
|
40,000 |
|
Expiration
Year
|
|
2058
|
|
|
2054
|
|
|
2051
|
|
|
2056
|
|
Production,
Warehouse, and Office
|
|
|
14,000 |
|
|
|
10,000 |
|
|
|
9,000 |
|
|
|
12,000 |
|
At this
time, our subsidiaries Haina and Tian Qing use an insignificant portion of our
facilities.
Item
3. Legal Proceedings.
We are
not a party to any material pending legal proceedings.
Item
4. Reserved.
PART
II
Item
5. Market for Common Equity, Related Stockholder Matters and Small
Business Issuer Purchases of Equity Securities.
Market
Information
Until May
28, 2008, our common stock was traded on FINRA’s Over-the-Counter Bulletin Board
under the trading symbol “CSKI.” On May 28, 2008, our common stock
commenced trading on the American Stock Exchange under the trading symbol
“CSY.” As of September 14, 2008, we terminated our listing on the
American Stock Exchange and became listed on the Nasdaq Global Market under the
trading symbol “CSKI.” Effective as of January 4, 2010, we qualified
to be listed on Nasdaq Global Select Market. The high and low sales
prices for our common stock in the fiscal years of 2009 and 2008 are as
follows:
|
|
Year Ended December 31, 2009
|
|
|
Year Ended December 31, 2008
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1st
Quarter
|
|
$ |
19.11 |
|
|
$ |
10.03 |
|
|
$ |
14.00 |
|
|
$ |
9.40 |
|
2nd
Quarter
|
|
$ |
17.80 |
|
|
$ |
10.21 |
|
|
$ |
17.10 |
|
|
$ |
9.50 |
|
3rd
Quarter
|
|
$ |
16.80 |
|
|
$ |
12.00 |
|
|
$ |
14.99 |
|
|
$ |
9.00 |
|
4th
Quarter
|
|
$ |
25.45 |
|
|
$ |
11.02 |
|
|
$ |
16.28 |
|
|
$ |
6.29 |
|
On March
15, 2010, the closing price for our common stock was $17.24.
Dividends
Since
inception, no dividends have been paid on our common stock. We intend
to retain any earnings for use in our business, so it is not expected that any
dividends on the common stock will be declared and paid in the foreseeable
future. We do not currently have any restrictions that would limit
our ability to pay dividends, and we are not currently aware of any restrictions
that are likely to limit our ability to pay dividends in the
future.
Holders
At March
15, 2010, there were 381 holders of record of our common stock, with 16,790,851
shares issued and outstanding. Such number of record owners was
determined from our shareholder records and does not include beneficial owners
whose shares are held in nominee accounts with brokers, dealers, banks and
clearing agencies.
Securities
Authorized For Issuance Under Equity Compensation Plan
As of
December 31, 2009, we had only one stock option, bonus, profit sharing, pension
or similar plan in place, which is our 2006 Stock Incentive Plan (the
“Plan”). The Plan reserves an aggregate of 1,500,000 shares of our
common stock for awards of stock options, stock appreciation rights, restricted
stock, performance stock and bonus stock granted thereunder. The
following table provides information as of December 31, 2009 with respect to the
shares of our common stock that may be issuable under our existing equity
compensation plans:
Equity
Compensation Plan Information
|
|
(a)
|
|
|
(b)
|
|
|
(c)
|
|
Plan Category
|
|
Number of securities
to be issued upon
exercise of
outstanding options,
warrants and rights
|
|
|
Weighted-
average exercise
price of
outstanding
options,
warrants and
rights
|
|
|
Number of
securities
remaining
available for future
issuance under
equity
compensation plans
(excluding
securities reflected
in column (a))
|
|
Equity
compensation plans approved by security holders (1)
|
|
|
0 |
|
|
$ |
- |
|
|
|
1,273,593 |
(3) |
Equity
compensation plans not approved by security holders (2)
|
|
|
0 |
|
|
|
N/A |
|
|
|
0 |
|
Total
|
|
|
0 |
|
|
$ |
- |
|
|
|
1,273,593 |
|
|
(1)
|
Our
board of directors adopted the 2006 Stock Incentive Plan (the “Plan”), to
be effective on July 31, 2006. The Plan was approved by the
shareholders on July 31, 2006.
|
|
(2)
|
We
do not have any equity compensation plans not approved by the security
holders.
|
|
(3)
|
The
Plan reserves an aggregate of 1,500,000 shares of our common stock for
awards of stock options, stock appreciation rights, restricted stock,
performance stock and bonus stock granted thereunder. We have
issued the following securities under the
Plan:
|
(a) In
October 2006, we granted stock options to purchase an aggregate of 113,500
shares of common stock to a total of 36 participants under the
Plan. In May 2009, an aggregate of 101,000 of these stock options
were exercised on a “cashless” basis by 36 participants, resulting in our
issuance of an aggregate of 75,888 shares. In August 2009, the
remaining 12,500 of these stock options were exercised on a
“cashless” basis by 9 participants, resulting in our issuance of an aggregate of
9,407 shares.
(b) In
April 2007, we issued an aggregate of 30,000 shares of restricted stock to a
total of 200 individuals under the Plan.
(c) In
July 2008, we issued an aggregate of 30,063 shares of restricted stock to a
total of 27 individuals under the Plan.
(d) In
December 2009, we issued an aggregate of 52,844 shares of restricted stock to a
total of 11 individuals under the Plan.
Recent
Sales of Unregistered Securities
The
following is a list of certain securities we sold or issued during fiscal
2008. There were no underwriting discounts or commissions paid
in connection with the sale of these securities, except as otherwise
noted. Certain information previously included in prior
Exchange Act reports we filed has not been furnished in this
report.
As of
December 26, 2009, we issued 52,844 “restricted” shares of our common stock to
certain employees, executive officers and directors of ours as consideration for
services pursuant to our 2006 Stock Incentive Plan.
We
believe the issuance of these shares was exempt from registration under the
Securities Act of 1933, as amended, pursuant to Section 4(2) and/or Regulation D
promulgated thereunder, as a transaction by an issuer not involving a public
offering.
Item
6. Selected Financial Data.
Restatement
of 2009 Financial Statements
As
discussed in Note 2 to the Financial Statements, the Company restated its
financial statements for the year ended December 31, 2009. On May 7,
2010, the Company determined that ASC 815-40, which was effective January 1,
2009, should have been applied to warrants issued in the Company’s 2008 private
placement, resulting in a reclassification of the warrants as a
derivative liability, measured at fair value, with changes in fair value
recognized as part of other income or expense for each reporting period
thereafter. In addition, the Company previously recorded a liability
in connection with certain registration rights provided to investors in the
private placement. On May 7, 2010, the Company determined that
because the obligations do not recognize cash settlement and the warrants can be
settled in unregistered shares, paragraphs 14 – 18 of EITF 00-19 do not apply to
the registration rights obligation. As a result, no liability is
required to be recorded with respect to this obligation and the Company has
recharacterized this previously recorded liability.
Key
financial data from the fiscal years ended December 2005 to 2009 is set forth in
the following table.
|
|
For the Years Ended December 31,
($ in thousands, except per share data)
|
|
|
|
2009
(restated)
|
|
|
2008
|
|
|
2007
|
|
|
2006
(restated)
|
|
|
2005
|
|
Operating
Data:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Revenues
|
|
$ |
130,092 |
|
|
$ |
91,816 |
|
|
$ |
49,318 |
|
|
$ |
19,882 |
|
|
$ |
7,712 |
|
Cost
of Goods Sold
|
|
|
31,671 |
|
|
|
22,403 |
|
|
|
10,940 |
|
|
|
5,063 |
|
|
|
2,214 |
|
Gross
Profit
|
|
|
98,421 |
|
|
|
69,413 |
|
|
|
38,379 |
|
|
|
14,819 |
|
|
|
5,498 |
|
Selling
expense
|
|
|
30,763 |
|
|
|
22,968 |
|
|
|
14,784 |
|
|
|
9,894 |
|
|
|
2,540 |
|
General
and administrative expense
|
|
|
4,191 |
|
|
|
2,514 |
|
|
|
1,380 |
|
|
|
844 |
|
|
|
735 |
|
Research
and development
|
|
|
14,960 |
|
|
|
7,413 |
|
|
|
3,158 |
|
|
|
2,027 |
|
|
|
64 |
|
Income
from Operations
|
|
|
46,251 |
|
|
|
35,659 |
|
|
|
18,614 |
|
|
|
1,932 |
|
|
|
2,462 |
|
Other
Income (Expense)
|
|
|
(4,768 |
) |
|
|
814 |
|
|
|
38 |
|
|
|
(228 |
) |
|
|
(18 |
) |
Provision
for income taxes
|
|
|
10,503 |
|
|
|
7,616 |
|
|
|
3,319 |
|
|
|
1,080 |
|
|
|
356 |
|
Net
Income
|
|
|
30,980 |
|
|
|
28,857 |
|
|
|
15,333 |
|
|
|
624 |
|
|
|
2,089 |
|
Basic
Earnings Per Share
|
|
|
1.87 |
|
|
|
1.91 |
|
|
|
1.27 |
|
|
|
0.05 |
|
|
|
0.19 |
|
Diluted
Earnings Per Share
|
|
|
1.86 |
|
|
|
1.87 |
|
|
|
1.15 |
|
|
|
0.05 |
|
|
|
0.19 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Balance
Sheet Data:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Total
Assets
|
|
$ |
140,363 |
|
|
$ |
101,259 |
|
|
$ |
37,285 |
|
|
$ |
16,681 |
|
|
$ |
8,992 |
|
Total
Current Liabilities
|
|
|
19,494 |
|
|
|
6,326 |
|
|
|
5,040 |
|
|
|
2,370 |
|
|
|
1,641 |
|
Working
Capital
|
|
|
56,895 |
|
|
|
49,509 |
|
|
|
15,447 |
|
|
|
7,798 |
|
|
|
2,858 |
|
Stockholder's
Equity
|
|
|
120,869 |
|
|
|
94,933 |
|
|
|
32,245 |
|
|
|
14,311 |
|
|
|
7,351 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Other
Data:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Net
cash provided by operating activities
|
|
$ |
33,449 |
|
|
$ |
27,538 |
|
|
$ |
11,601 |
|
|
$ |
5,183 |
|
|
$ |
1,090 |
|
Net
Cash used in investing activities
|
|
|
(21,154 |
) |
|
|
(23,115 |
) |
|
|
(10,261 |
) |
|
|
(4,597 |
) |
|
|
(776 |
) |
Net
Cash provided by (used in) financing activities
|
|
|
29 |
|
|
|
25,355 |
|
|
|
(33 |
) |
|
|
(2,931 |
) |
|
|
591 |
|
Item
7. Management’s Discussion and Analysis of Financial Condition and
Results of Operation.
The
financial and business analysis in this Annual Report on Form 10-K (the
“Report”) provides information we believe is relevant to an assessment and
understanding of our financial condition and results of operations. The
following discussion should be read in conjunction with our consolidated
financial statements and related notes included in Part II, Item 8 of this
Report.
FORWARD
LOOKING STATEMENTS
The
following discussion should be read in conjunction with the information
contained in our consolidated financial statements and the notes thereto
appearing elsewhere herein and in the risk factors and “Forward Looking
Statements” summary set forth in the forepart of this Annual Report as well as
the “Risk Factors” section above and are afforded the safe harbor provisions of
Section 27A of the Securities Act and Section 21E of the Securities Exchange Act
of 1934, as amended. Readers should carefully review the risk factors disclosed
in this Annual Report and other documents filed by us with the
SEC.
DISCUSSION
We are
engaged, through our China-based indirect subsidiaries described below, in the
development, manufacture, marketing and sale of over-the-counter, branded
nutritional supplements and over-the-counter plant and herb-based pharmaceutical
and medicinal products. Our principal products are external use
TCMs. We have evolved into an integrated manufacturer, marketer and
distributor of external-use TCM products sold primarily in the PRC and through
Chinese domestic pharmaceutical chains. Recently, we have been
expanding our worldwide sales effort as well. Prior to 2009, we sold
both our own manufactured products, as well as medicinal and pharmaceutical
products manufactured by others on a contract basis, categorized by us as
Contract Sales. Commencing in 2009, we discontinued all of our
Contract Sales as part of our revised strategic plan.
In
2009, we achieved continued growth on the sale of our own product line through
our sustained efforts to expand our distribution channels and promote our
products. For the year ended December 31, 2009, total revenues were
$130,092,000, compared to $91,816,000 and $49,318,000 for the years ended
December 31, 2008 and 2007, respectively. Net income was $30,980,000, or $1.86
per share, in 2009, compared to net income of $28,857,000, or $1.87 per share,
in 2008, and net income of $15,333,000, or $1.15 per share, in 2007, as
calculated on a diluted basis for all periods presented.
All of
our business is conducted through our wholly-owned subsidiary, ACPG which, in
turn, wholly owns Harbin TDR, and TDR’s subsidiaries.
Recent
Developments
On April
3, 2008, TDR completed its acquisition of Tianlong, a company that had a variety
of medicines approved by the SFDA and new medicine applications, and which was
in the business of manufacturing external-use pharmaceuticals. TDR
previously acquired the Beijing sales office of Tianlong in
mid-2006. In connection with this transaction, TDR acquired 100% of
the issued and outstanding capital stock of Tianlong from its sole stockholder,
in consideration for an aggregate purchase price of approximately $8,300,000,
consisting of $8,000,000 in cash, and 23,850 shares of our common stock (valued
at $12.00 per share).
On April
18, 2008, TDR consummated its acquisition of Haina, licensed as a wholesaler of
TCM, bio-products, medicinal devices, antibiotics and chemical
medicines. Haina did not have an established sales network and was
acquired for its primary asset, a GSP license issued by the Heilongjiang
Province office of the SFDA. The SFDA only issues such licenses to
pharmaceutical resellers that maintain certain quality control
standards. The GSP license was issued as of December 21, 2006 and
will expire on January 29, 2012. This GSP license has enabled us to
expand our sales of medicinal products without having to go through a lengthy
license application process. In connection with this transaction, TDR
acquired 100% of the issued and outstanding capital stock of Haina from its
three stockholders in consideration for payment of approximately
$437,000.
On
September 5, 2008, TDR acquired Peng Lai, from Peng Lai Jin Chuang Group
Corporation. Peng Lai, which has received Good Manufacturing Practice
(“GMP”) certification from the SFDA, was organized to develop, manufacture and
distribute pharmaceutical, medicinal and diagnostic products in the
PRC. In connection with this transaction, TDR acquired all of Peng
Lai’s assets, including, without limitation, franchise, production and operating
rights to a portfolio of twenty (20) medicines approved by the SFDA, for an
aggregate purchase price of approximately $7,000,000 million, consisting of
approximately $2,500,000 million in cash, and 381,606 shares of our common stock
(valued at $12.00 per share).
Trends
and Uncertainties
In 2008,
general worldwide economic conditions declined due to sequential effects of the
sub prime lending crisis, general credit market crisis, collateral effects on
the finance and banking industries, concerns about inflation, slower economic
activity, decreased consumer confidence, reduced corporate profits and capital
spending, adverse business conditions and liquidity
concerns. However, since all of our business operations, and most of
our sales, are currently conducted in the PRC, we have not been greatly affected
by the economic downtown.
We have
benefited from the overall economic development in the PRC in recent years and
the increase in the number of elderly people in China, which together have
resulted in increased expenditures on medicine in the PRC, including
TCMs.
In fiscal
2007, our sales model was focused on the creation of our own distribution
channels. Therefore, we sold products directly to many smaller
distributors and retail store locations. In fiscal 2008, we changed
our business model and entered into distribution agreements with larger regional
sales agents, who resell to smaller distributors and retail store
locations. In addition, we entered into contracts with nationwide
chain pharmacies, such as Nepstar, Tong Ren Tang, Jin Xiang, and Ren Min Tong
Tai. Through the extensive sales networks of these nationwide chains,
we are able to reach all major metropolitan areas throughout the
PRC. These changes to our product distribution channels resulted in
our direct customer base decreasing from 943 customers at December 31, 2007 to
212 customers at December 31, 2009.
Our
change of sales strategy in fiscal 2008 was initiated to improve product channel
efficiencies, and to give us access to an increased number of ultimate
purchasers. We believe that these changes will lead to further
increased revenue by extending the reach of its distribution
network. We also believe that, by reducing the number of customers we
sell to directly, we will be able to streamline our accounts receivable
management and collection, and reduce channel distribution
costs. These favorable cost variances are expected to be partially
offset by product price incentives we grant to the larger agents with which we
have contracted.
In fiscal
2007, 26.4% of our total revenues, or $12,998,000, was attributable to sales of
other manufacturers’ products through Contract Sales. One of the main
manufacturers for which we resold products was Tianlong. On April 3,
2008, we acquired Tianlong and were able to fully integrated Tianlong’s
products, which we had been previously selling on a contract basis, into our
marketing and distribution channels. Following the acquisition of
Tianlong we continued to phase out our Contract Sales and, as of the end of
fiscal 2008, we no longer sell other company’s products on a contract
basis.
Historically,
we signed agreements with suppliers that allowed us to hold extra raw materials
at the cost of the suppliers. As a result, we were able to minimize
our own inventory carrying costs, and improve our cash management, by keeping
the inventory at the minimum level required to support the short-term
sales. However, due to the forecasts for certain cost increases of
raw materials in fiscal 2010, we began to increase our inventory levels toward
the second half of 2009.
Results
of Operations
Restatement
of Financial Statements
As
discussed in Note 2 to the Financial Statements, the Company restated its
financial statements for the year ended December 31, 2009. On May 7,
2010, the Company determined that ASC 815-40, which was effective January 1,
2009, should have been applied to warrants issued in the Company’s 2008 private
placement, resulting in a reclassification of the warrants as a derivative
liability, measured at fair value, with changes in fair value recognized as part
of other income or expense for each reporting period thereafter. In
addition, the Company previously recorded a liability in connection with certain
registration rights provided to investors in the private
placement. On May 7, 2010, the Company determined that because the
obligations do not recognize cash settlement and the warrants can be settled in
unregistered shares, paragraphs 14 – 18 of EITF 00-19 do not apply to the
registration rights obligation. As a result, no liability is required
to be recorded with respect to this obligation and the Company has
recharacterized this previously recorded liability.
For
the years ended December 31, 2009, 2008 and 2007
Revenue,
Cost of Goods Sold Gross Profit and Gross Profit Margin
The
following table sets forth our revenues, cost of goods sold, gross
profit and gross profit margin during the fiscal years ended December 31, 2009,
2008, and 2007:
|
|
For the Years Ended December 31,
($ in thousands)
|
|
|
|
2009
|
|
|
Variance
|
|
|
2008
|
|
|
Variance
|
|
|
2007
|
|
Revenues
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Product
Sales (net of sales allowance)
|
|
$ |
130,092 |
|
|
|
51 |
% |
|
$ |
86,161 |
|
|
|
137 |
% |
|
$ |
36,320 |
|
Contract
Sales
|
|
|
0 |
|
|
|
- |
|
|
|
5,655 |
|
|
|
(57 |
)% |
|
|
12,998 |
|
Total
Revenues
|
|
$ |
130,092 |
|
|
|
42 |
% |
|
$ |
91,816 |
|
|
|
86 |
% |
|
$ |
49,318 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost
of Goods Sold
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Cost
of goods sold
|
|
|
31,671 |
|
|
|
41 |
% |
|
|
22,403 |
|
|
|
105 |
% |
|
|
10,940 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Gross
Profit
|
|
$ |
98,422 |
|
|
|
42 |
% |
|
$ |
69,413 |
|
|
|
81 |
% |
|
$ |
38,378 |
|
Gross
Profit Margin
|
|
|
75.7 |
% |
|
|
|
|
|
|
75.6 |
% |
|
|
|
|
|
|
77.8 |
% |
Year
over year – 2009 to 2008
Total
revenues increased by approximately $38,276,000, or 42%, from approximately
$91,816,000 in the fiscal year ended December 31, 2008, to approximately
$130,092,000 for the fiscal year ended December 31, 2009. The
increase in our revenues is primarily attributable to increase in our product
sales related to:
|
·
|
strong
performances from our sales distribution channels, obtained by our hiring
of additional direct territory managers and sales
agents;
|
|
·
|
our
efforts to locate and cooperate with more reputable distributors for
certain of our products;
|
|
·
|
the
increase in marketing and advertising expenditures of approximately
$7,228,000, or 99%, from approximately $7,299,000 in fiscal 2008 to
approximately $14,527,000 in fiscal 2009;
and
|
|
·
|
the
full-year effect of sales of products of Tianlong, which generated
approximately $43,138,000 and approximately $13,803,000 in 2009 and 2008,
respectively, and Peng Lai, which generated approximately $11,188,000 and
approximately $2,164,000 in 2009 and 2008, respectively, two of the
businesses we acquired in fiscal
2008.
|
The
increase in our product sales were partially offset by our discontinuance of all
Contract Sales in fiscal 2009, which we began to phase out in fiscal
2008.
Cost of
goods sold increased by approximately $9,268,000, or 41%, to approximately
$31,671,000 in fiscal 2009 compared to the prior year. This increase
was directly related to an increase in sales.
Gross
profit increased by 42%, from approximately $69,413,000 in 2008 to approximately
$98,422,000 in 2009. Our gross margin remained constant at
approximately 76%.
Year
over year – 2008 to 2007
Total
revenues increased by approximately $42,498,000, or 86%, from approximately
$49,318,000 in the fiscal year ended December 31, 2007, to approximately
$91,816,000 for the fiscal year ended December 31, 2008. The increase
in revenue is primarily attributable to strong performances from our sales
distribution channels, and our sales of products of Tianlong and Peng Lai, which
we acquired in fiscal 2008.
Product
sales increased by 137% in the year ended December 31, 2008, to approximately
$86,161,000 from approximately $36,320,000 in 2007. This growth in
sales is attributable to volume and our efforts to continue to develop our
distribution channels by hiring additional direct territory managers and sales
agents to assure that our products and their associated benefits are seen by
those making or influencing the purchasing decisions, and our sales of products
of Tianlong and Peng Lai, which we acquired in fiscal 2008.
Contract
sales of non-manufactured products amounted to approximately $5,655,000 in the
year ended December 31, 2008, or a significant decrease of approximately
$7,343,000 from sales of approximately $12,998,000 in 2007.
In 2007,
our sales model was focused on the creation of our own distribution
channels. Therefore, we sold products directly to many smaller
distributors and retail store locations. In 2008, we changed our
business model and entered into distribution agreements with larger regional
sales agents, which resell to smaller distributors and retail store
locations. In addition, we began entering into contracts with
nationwide chain pharmacies. In 2008, TDR began to discontinue
contract sales as part of its strategic goals.
Our
change of sales strategy in fiscal 2008 was initiated to improve product channel
efficiencies, and to give us access to an increased number of ultimate
purchasers. We believe that these changes will lead to further
increased revenue by extending the reach of our distribution
network. We also believe that, by reducing the number of customers we
sell to directly, we will be able to streamline our accounts receivable
management and collection, and reduce channel distribution
costs. These favorable cost variances are expected be partially
offset by product price incentives we grant to the larger agents with which we
have contracted.
Cost of
goods sold increased by approximately $11,464,000, or 105%, from approximately
$10,940,000 in the year ended December 31, 2007, to approximately $22,403,000
for the year ended December 31, 2008, as a direct result of increased sales
activities, partially offset by a higher gross margin on our sales of Tianlong
products following the acquisition in April 2008. Overall, our product gross
margins decreased slightly to 76% for the year ended December 31, 2008 from 78%
for the year ended December 31, 2007. From January 1, 2008 thought April 2,
2008, revenues from Tianlong contract sales were approximately $1,477,000, and
gross profit from these sales were approximately $1,173,000. The gross margin
from these sales were approximately 79.4%, After our acquisition of Tianlong,
revenues from sales of Tianlong products were approximately $13,803,000, and
gross profit from these sales were approximately $12,298,000. The gross margin
from these sales was approximately 89.1%. This increase in gross margin from
sales of Tianlong’s products following the acquisition was offset by the
decrease in gross margins related to sales of certain TDR’s products due to our
reduction in the sales prices of certain of our products to be competitive in
the PRC market.
Sales
by Product Line
We
believe that the most meaningful presentation of our products is by categories
of method of delivery. The following table sets forth our principal product
categories based on application type, and the approximate amount and percentage
of revenue from each of such product categories, during each of the fiscal years
ended December 31, 2009, 2008, and 2007:
|
|
For the Years Ended December
31
($ in thousands)
|
|
|
|
2009
|
|
|
2008
|
|
|
2007
|
|
Product Category
|
|
Sales
|
|
|
% of
Sales
|
|
|
Sales
|
|
|
% of
Sales
|
|
|
Sales
|
|
|
% of
Sales
|
|
Patches
|
|
$ |
40,770 |
|
|
|
31.3 |
% |
|
$ |
35,484 |
|
|
|
38.6 |
% |
|
$ |
19,609 |
|
|
|
39.9 |
% |
Ointments
|
|
|
28,862 |
|
|
|
22.2 |
% |
|
|
23,068 |
|
|
|
25.1 |
% |
|
|
3,270 |
|
|
|
12.6 |
% |
Sprays
|
|
|
18,499 |
|
|
|
14.2 |
% |
|
|
10,613 |
|
|
|
11.6 |
% |
|
|
8,742 |
|
|
|
18.7 |
% |
Diagnostic
Kits
|
|
|
10,239 |
|
|
|
7.9 |
% |
|
|
8,781 |
|
|
|
9.6 |
% |
|
|
2,994 |
|
|
|
6.1 |
% |
Contract
Sales
|
|
|
0 |
|
|
|
0.0 |
% |
|
|
5,655 |
|
|
|
6.2 |
% |
|
|
12,998 |
|
|
|
16.6 |
% |
Others
|
|
|
31,722 |
|
|
|
24.4 |
% |
|
|
8,215 |
|
|
|
8.9 |
% |
|
|
1,705 |
|
|
|
6.2 |
% |
Total
|
|
$ |
130,092 |
|
|
|
100.0 |
% |
|
$ |
91,816 |
|
|
|
100.0 |
% |
|
$ |
49,318 |
|
|
|
100.0 |
% |
Year
over year – 2009 to 2008
During
the fiscal year ended December 31, 2008, we acquired Tianlong (April
2008), Haina (April 2008) and Peng Lai (September 2008). Our revenues
increased in 2009 compared to 2008, primarily due to our cooperation with more
reputable sales agents and distributors, which have been able to put our
products in more extensive sales networks, and the full-year effect of sales of
products of Tianlong and Peng Lai, two of the businesses we acquired in fiscal
2008. As a result of signing agreements with these distributors, the
sales revenues for products in the patches, sprays, and diagnostic kits
categories increased 14.9%, 74.3%, and 16.6% year over year. The
revenue increase of approximately $5,794,000 in the ointment category, and the
revenue increase of approximately $23,507,000 in other products
category, are primarily due to our increased spending in marketing and
advertising for certain products in these categories. Tianlong’s
products generated approximately $43,138,000 and $13,803,000 in 2009 and
2008, respectively. Revenue generated by Tianlong’s products are
included in the ointment, spray and other product categories. Peng
Lai’s products generated approximately $11,188,000 and $2,164,000 in 2009 and
2008, respectively. Revenue generated by Peng Lai’s products are
included in the other product category. These increases were
partially offset by a decrease in our contract sales of approximately
$5,655,000, due to our discontinuance of all contract sales as of January 1,
2009.
Out of
the 91 products we commercialized in fiscal year 2009, 10 products accounted for
approximately 68% of the total revenue. Out of the 97 products we
commercialized in fiscal year 2008, 10 products accounted for approximately 72%
of total revenue.
Year
over year – 2008 to 2007
Our
increase in revenues in 2008 as compared to 2007 was due to a combination of our
sale of products of Tianlong and Peng Lai, two of the businesses we acquired in
fiscal 2008, as well as our internal growth driven by increases in the revenues
of TDR and First.
Our
internal growth was driven by increases in the revenues of TDR, which increased
from $33,326,000 in 2007 to $60,078,000 in 2008 and First, which increased from
approximately $2,994,000 in 2007 to approximately $8,781,000 in
2008. These increases were partially offset by a decrease in our
contract sales of approximately $7,358,000, or 57% from approximately
$12,998,000 in fiscal 2007 to approximately $5,640,000 in fiscal 2008, due
primarily to our discontinuance of contract sales of Tianlong products following
the acquisition of Tianlong as of April 3, 2008.
In
2008, before TDR acquired Tianlong, the majority of our contracts sales
consisted of products purchased from Tianlong. In 2008, TDR began to discontinue
contract sales, and in 2009, TDR discontinued contract sales as part of its
strategic goals and, in 2009 TDR discontinued contact sales. Revenues derived
from the sale of Tianlong products of approximately $4,805,000 and approximately
$1,477,000 for 2007 and 2008 respectively, have been reallocated to each of
the appropriate product categories to present a more appropriate measure of our
revenues by product line.
Following
the Tianlong acquisition, we were able to fully integrate Tianlong’s products
into our marketing and distribution channels and increase overall
sales. As a result, we derived an aggregate of approximately
$13,803,000 from the sale of Tianlong’s products for the remainder of 2008, in
addition to approximately $1,447,000 of contract sales of Tianlong’s products
from January 1, 2008 through the Tianlong acquisition.
Prior to
our acquisition of Peng Lai, as of September 5, 2008, Peng Lai had nominal
production and operations. Following the acquisition, Peng Lai
contributed revenue of approximately $2,164,000 to our total revenue in
2008.
Haina did
not have an established sales network and was acquired only for its GSP
license.
Operating
Expenses
The
following table summarizes the changes in our operating expenses for the years
ended December 31, 2009, 2008 and 2007:
|
|
For the Years ended December
31,
($ in
thousands)
|
|
|
|
2009
|
|
|
Variance
|
|
|
2008
|
|
|
Variance
|
|
|
2007
|
|
Operating
Expenses
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Selling
expense
|
|
$ |
30,763 |
|
|
|
34 |
% |
|
$ |
22,969 |
|
|
|
55 |
% |
|
$ |
14,784 |
|
General
and administrative expense
|
|
|
4,191 |
|
|
|
67 |
% |
|
|
2,514 |
|
|
|
82 |
% |
|
|
1,380 |
|
Depreciation
and amortization
|
|
|
2,255 |
|
|
|
163 |
% |
|
|
858 |
|
|
|
94 |
% |
|
|
443 |
|
Research
and development
|
|
|
14,960 |
|
|
|
102 |
% |
|
|
7,413 |
|
|
|
135 |
% |
|
|
3,158 |
|
Total
operating expenses
|
|
$ |
52,170 |
|
|
|
55 |
% |
|
$ |
33,754 |
|
|
|
71 |
% |
|
$ |
19,765 |
|
Percentage
of operating expenses to revenue
|
|
|
40.1 |
% |
|
|
|
|
|
|
36.8 |
% |
|
|
|
|
|
|
40.1 |
% |
Year
over year – 2009 to 2008
Total
operating expenses increased by approximately $18,416,000, or 55%, from
approximately $33,754,000 in the fiscal year ended December 31, 2008, to
approximately $52,170,000 for the fiscal year ended December 31,
2009.
Selling
expenses increased by approximately $7,794,000 in 2009 compared with 2008. This
increase was primarily related to increased costs of advertising from
approximately $7,299,000 in 2008 to approximately $14,527,000 in 2009, resulting
from our increased marketing and sales efforts.
General
and administrative expenses for the year ended December 31, 2009 increased
approximately $1,677,000, or 67%, compared with 2008. This increase
was primarily due to an expense for share-based compensation, of approximately
$1,242,000, for common shares we issued in December 2009 ($316,000 in
2008).
Depreciation
and amortization expenses in 2009 increased by approximately $1,397,000, or
163%, compared with 2008. This increase was primarily due
to:
|
·
|
the
amortization of certain proprietary technologies we acquired in the fourth
quarter of fiscal 2008, in the amount of approximately $6.6 million, which
are amortized over a period of 10 years;
and
|
|
·
|
the
full year effect of depreciation and amortization of tangible and
intangible assets we acquired in the business acquisitions we consummated
in fiscal 2008, in the amount of approximately $15.7
million.
|
Research
and development expenses were approximately $14,960,000 in the year ended
December 31, 2009, compared to approximately $7,413,000 for 2008. The
increased R&D expenses in 2009 were primarily due to our research and
development of certain proprietary technologies.
Set
forth below is certain information regarding our major research and development
projects in 2009. The additional costs and expected completion dates
set forth in the table below are subject to change, which may be material, based
on various factors, many of which are out of our control:
Projects
|
|
Stage
|
|
2008 Expense
|
|
|
2009 Expense
|
|
|
Aggregate
Expenses Since
Commencement of
Project
|
|
|
Estimated
Additional Costs to
Complete Research
and Development
|
|
Remaining Activities and Expected Research and
Development Completion Date***
|
Diagnostic Kits -
19 products*
|
|
Clinical trial
|
|
$ |
2,261,000 |
|
|
$ |
2,727,000 |
|
|
$ |
4,988,000 |
|
|
|
$800,000 |
|
13
projects are estimated to be submitted to the SFDA in later half of 2010,
with an estimated aggregate cost of $500,000; Another 6 products are
estimated to complete clinical trial in fiscal 2010, then get into the
stage of long term stability testing through 2013, with estimated cost of
$300,000
|
Injections
- 6 projects
|
|
Clinical
trial
|
|
$ |
614,000 |
|
|
$ |
1,944,000 |
|
|
$ |
2,558,000 |
|
|
|
$300,000 |
|
One
product is pending SFDA approval; 3 products are planned to be submitted
to the SFDA within fiscal 2010, with an estimated cost of $100,000; The
other 2 products are going into long term stability testing stage with an
estimated cost of $200,000
|
Breast
Cancer Technology
|
|
Efficacy
testing, Acute and Long Term Toxicity testing
|
|
$ |
0 |
|
|
$ |
2,272,000 |
|
|
$ |
2,272,000 |
|
|
|
$8.3
million
|
|
Efficacy
stage has been completed in 2009, long term stability testing is estimated
to be completed during the first half of 2011, with an estimated cost of
$300,000, then apply to the SFDA for getting into the clinical trial. The
clinical trial is estimated to be completed in 2015, with an
estimated cost of $6-8 million, afterwards, we intend to apply to the SFDA
to enter into the production stage.
|
Patches
- 4 products
|
|
Extraction
optimization testing
|
|
$ |
0 |
** |
|
$ |
1,820,000 |
|
|
$ |
1,820,000 |
|
|
$ |
** |
Completed
|
Monoclonal
Antibody
|
|
Completed
|
|
$ |
948,000 |
|
|
$ |
965
,000 |
|
|
$ |
1,913,000 |
|
|
$1.8
to $2 million
|
|
Continue
study in 2010; does not require SFDA approval
|
Endostatin
|
|
Efficacy
testing, Acute and Long Term Toxicity testing
|
|
$ |
1,192,000 |
|
|
$ |
439,000 |
|
|
$ |
1,631,000 |
|
|
$8
to $10 million
|
|
Clinical
trials; estimated to be completed in 2016 and submitted for SFDA
approval
|
Antroquinonol
|
|
Clinical
trial
|
|
$ |
0 |
|
|
$ |
387,000 |
|
|
$ |
387,000 |
|
|
$16 to $18 million
|
|
Efficiency,
acute and long-term toxicity testing; pre-clinical and clinical trials are
estimated to be completed in 2018 and submitted for SFDA
approval
|
Radix Isatidis
granule and
syrup
|
|
Production
process optimization
|
|
$ |
0 |
|
|
$ |
282,000 |
|
|
$ |
282,000 |
|
|
|
$400,000 - $500,000 |
|
Estimated
to be completed in 2010
|
Naftopidil
Dispersible tablets
|
|
Production
process optimization
|
|
$ |
0 |
|
|
$ |
256,000 |
|
|
$ |
256,000 |
|
|
|
$400,000 - $500,000 |
|
Estimated
to be completed in 2010
|
Sertraline
Hydrochloride capsules
|
|
Production
process optimization
|
|
$ |
0 |
|
|
$ |
249,000 |
|
|
$ |
249,000 |
|
|
|
$400,000 - $500,000 |
|
Estimated
to be completed in
2010
|
*
During 2008, we conducted long-term stability testing on clinical trials
on a total of 13 projects for an aggregate expense of $2,261,000. We
spent an immaterial amount on further research and development of the projects
in 2009 and expect to submit those projects for SFDA approval during the second
half of 2010 at an estimated aggregate additional expense of
$500,000.
**
The amount is not meaningful.
*** Does
not include time required for SFDA approval, if any.
In
addition to the projects set forth in the table above, we commenced clinical
trials or efficacy, acute and long-term toxicity testing on several other
projects. We expect to complete testing and/or trials for these
projects between 2012 and 2014 at an estimated cost of $600,000 to $1,000,000
per project.
Other
Income
For
the year ended December 31, 2009 (restated), we incurred a charge of $4,807,000
due to the change in fair value of a derivative warrant liability resulting from
an increase in the fair value of warrants issued in the Offering (as defined
under the caption “ – Private Offering”).
Year
over year – 2008 to 2007
Total
operating expenses increased by approximately $13,989,000, or 71%, from
approximately $19,765,000 in the fiscal year ended December 31, 2007, to
approximately $33,754,000 for the fiscal year ended December 31,
2008.
Selling
expenses increased by approximately $8,185,000 in 2008 compared with
2007. The higher selling expenses are primarily related
to:
|
·
|
increased
costs of advertising, from approximately $4,385,000 in 2007, to
approximately $7,299,000 in 2008;
and
|
|
·
|
increased
sales commissions resulting from our increased
revenues.
|
General
and administrative expenses for the year ended December 31, 2008 increased
approximately $1,134,000, or 82%, over the 2007. The higher general
and administrative expenses are primarily due to the increases in salaries and
other administrative expenses resulting from the business acquisitions we made
in fiscal 2008. In 2008, we recorded share-based compensation expense
of $316,000, as compared to $235,000 in 2007.
Depreciation
and amortization in 2008 increased by approximately $415,000 compared
2008. The higher depreciation and amortization expenses are primarily due to the
increased tangible and intangible assets we acquired through the business
acquisitions we consummated in 2008.
We
conduct our research and development activities both internally and through
collaborative arrangements with universities and research
institutions. Our research and development expenses were
approximately $7,413,000 in the year ended December 31, 2008, compared to
approximately $3,158,000 in the year ended December 31, 2007. The increased
R&D expenses in 2008 were primarily due to our taking over of the ongoing
research and development projects in Tianlong and Peng Lai because of these two
acquisitions and other technologies we acquired in 2008 and 2009. We
also increased our research and development activities relating to certain
previously developed technologies.
Historically,
our internal research and development activities have been conducted at our
research, development and laboratory facilities located at the principal
business offices of its wholly-owned subsidiary, TDR. In 2007, our
research and development projects consisted of a total of eight diagnostic kits.
These bio-engineering projects were conducted by TDR’s wholly-owned
subsidiary, First. In 2008, we spent an immaterial amount on research
and development for these eight products, of which:
|
·
|
we
received approval by the SFDA of our Ovulation Diagnostic
Kit;
|
|
·
|
our
Prostate Cancer Diagnostic Kit and Urine Micro-Albumin Colloid Gold
Diagnostic Kit were submitted to the SFDA for approval;
and
|
|
·
|
the
remaining five products were undergoing long-term stability testing while
we provided supplemental documentation to the SFDA for these
projects.
|
As
previously discussed, in fiscal 2008 we acquired Tianlong and Peng
Lai. As a result, we had 47 projects in development in fiscal
2008. Set forth below is a table of our research and development
expenses for 2008, classified by product category and stage of
development:
|
|
|
|
Stage
of Development by Number of Projects and U.S. Dollar
Amount
($
in
thousands)
|
|
Category
|
|
|
|
Application
and Efficacy
|
|
|
Acute and
Long Term
Toxicity
|
|
|
Long Term
Stability
|
|
|
Pending
SFDA
Approval
|
|
|
Supplemental
Documentation
|
|
|
SFDA
Approval
|
|
|
TOTAL
|
|
Bio-Engineering
(a)
|
|
# |
|
|
1 |
(b) |
|
|
1 |
(c) |
|
|
13 |
|
|
|
2 |
|
|
|
- |
|
|
|
1 |
|
|
|
18 |
|
|
$ |
|
$ |
948 |
|
|
$ |
1,192 |
|
|
$ |
2,261 |
|
|
|
- |
|
|
-
|
|
|
|
- |
|
|
$ |
4,401 |
|
Eye
Drops
|
|
# |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
2 |
|
|
|
2 |
|
|
$ |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
$ |
103 |
|
|
$ |
103 |
|
Nasal
Drops
|
|
# |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
1 |
|
|
|
1 |
|
|
$ |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
$ |
61 |
|
|
$ |
61 |
|
Injections
|
|
# |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|
|
1 |
|
|
|
- |
|
|
|
4 |
|
|
|
5 |
|
|
$ |
|
|
- |
|
|
|
- |
|
|
|
- |
|
|