СÖíÊÓƵapp

Table of Contents

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, DC 20549

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FORM 10-Q

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(Mark One)

x QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended MarchÌý31, 2012.

OR

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¨ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý to ÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌýÌý.

Commission file number 001-33528

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СÖíÊÓƵapp Health, Inc.

(Exact Name of Registrant as Specified in Its Charter)

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Delaware Ìý 75-2402409

(State or Other Jurisdiction of

Incorporation or Organization)

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(I.R.S. Employer

Identification No.)

4400 Biscayne Blvd.

Miami, FL 33137

(Address of Principal Executive Offices) (Zip Code)

(305)Ìý575-4100

(RegistrantÂ’s Telephone Number, Including Area Code)

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Indicate by check mark whether the registrant: (1)Ìýhas filed all reports required to be filed by SectionÌý13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12Ìýmonths (or for such shorter period that the registrant was required to file such reports), and (2)Ìýhas been subject to such filing requirements for the past 90Ìýdays.ÌýÌýÌýÌýxÌýÌýYESÌýÌýÌýÌý¨ÌýÌýNO

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 during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such files).ÌýÌýÌýÌýYESÌýÌýxÌýÌýÌýÌýNOÌýÌý¨

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller reporting company. See the definitions of “large accelerated filer,” “accelerated filer” and “smaller reporting company” (in RuleÌý12b-2 of the Exchange Act) (Check one):

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LargeÌýacceleratedÌýfiler Ìý ¨ ÌýÌý AcceleratedÌýfiler Ìý x
Non-accelerated filer Ìý ¨ÌýÌý(Do not check if a smaller reporting company) ÌýÌý SmallerÌýreportingÌýcompany Ìý ¨

Indicate by check mark whether the registrant is a shell company (as defined in RuleÌý12b-2 of the Exchange Act):ÌýÌýÌýÌýYESÌýÌý¨ÌýÌýÌýÌýNOÌýÌýx

As of MayÌý1, 2012, the registrant had 295,126,572 shares of common stock outstanding.

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Table of Contents

TABLE OF CONTENTS

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PART I. FINANCIAL INFORMATION

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ItemÌý1. Financial Statements

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Condensed Consolidated Balance Sheets as of March 31, 2012 and December 31, 2011 (unaudited)

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Condensed Consolidated Statements of Operations for the three months ended March 31, 2012 and March 31, 2011 (unaudited)

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Condensed Consolidated Statements of Comprehensive Loss for the three months ended March 31, 2012 and March 31, 2011 (unaudited)

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Condensed Consolidated Statements of Cash Flows for the three months ended March 31, 2012 and March 31, 2011 (unaudited)

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Notes to Financial Statements

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ItemÌý2. ManagementÂ’s Discussion and Analysis of Financial Condition and Results of Operations

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ItemÌý3. Quantitative and Qualitative Disclosures About Market Risk

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ItemÌý4. Controls and Procedures

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PART II. OTHER INFORMATION

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ItemÌý1. Legal Proceedings

ÌýÌý Ìý 30 ÌýÌý

ItemÌý1A. Risk Factors

ÌýÌý Ìý 30 ÌýÌý

ItemÌý2. Unregistered Sales of Equity Securities and Use of Proceeds

ÌýÌý Ìý 30 ÌýÌý

ItemÌý3. Defaults Upon Senior Securities

ÌýÌý Ìý 30 ÌýÌý

ItemÌý4. Mine Safety Disclosures

ÌýÌý Ìý 30 ÌýÌý

ItemÌý5. Other Information

ÌýÌý Ìý 30 ÌýÌý

ItemÌý6. Exhibits

ÌýÌý Ìý 30 ÌýÌý

Signatures

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Exhibit Index

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EX-31.1 SectionÌý302 Certification of CEO

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EX-31.2 SectionÌý302 Certification of CFO

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EX-32.1 SectionÌý906 Certification of CEO

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EX-32.2 SectionÌý906 Certification of CFO

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CAUTIONARY STATEMENT REGARDING FORWARD-LOOKING STATEMENTS

This Quarterly Report on Form 10-Q contains “forward-looking statements,” as that term is defined under the Private Securities Litigation Reform Act of 1995 (“PSLRA”), SectionÌý27A of the Securities Act of 1933, as amended, and SectionÌý21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements include statements about our expectations, beliefs or intentions regarding our product development efforts, business, financial condition, results of operations, strategies or prospects. You can identify forward-looking statements by the fact that these statements do not relate strictly to historical or current matters. Rather, forward-looking statements relate to anticipated or expected events, activities, trends or results as of the date they are made. Because forward-looking statements relate to matters that have not yet occurred, these statements are inherently subject to risks and uncertainties that could cause our actual results to differ materially from any future results expressed or implied by the forward-looking statements. Many factors could cause our actual activities or results to differ materially from the activities and results anticipated in forward-looking statements. These factors include those described below and in “Item 1A-Risk Factors” of our Annual Report on Form 10-K for the year ended DecemberÌý31, 2011, and described from time to time in our other reports filed with the Securities and Exchange Commission. Except as required by law, we do not undertake any obligation to update forward-looking statements. We intend that all forward-looking statements be subject to the safe-harbor provisions of the PSLRA. These forward-looking statements are only predictions and reflect our views as of the date they are made with respect to future events and financial performance.

Risks and uncertainties, the occurrence of which could adversely affect our business, include the following:

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We have a history of operating losses and we do not expect to become profitable in the near future.

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Our technologies are in an early stage of development and are unproven.

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Our business is substantially dependent on our ability to develop, launch and generate revenue from our pharmaceutical and diagnostic programs.

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Our research and development activities may not result in commercially viable products.

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The results of previous clinical trials may not be predictive of future results, and our current and planned clinical trials may not satisfy the requirements of the FDA or other non-U.S. regulatory authorities.

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We will require substantial additional funding, which may not be available to us on acceptable terms, or at all.

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We expect to finance future cash needs primarily through public or private offerings, debt financings or strategic collaborations, which may dilute your stockholdings in the Company.

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If our competitors develop and market products that are more effective, safer or less expensive than our future product candidates, our commercial opportunities will be negatively impacted.

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The regulatory approval process is expensive, time consuming and uncertain and may prevent us or our collaboration partners from obtaining approvals for the commercialization of some or all of our product candidates.

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Failure to recruit and enroll patients for clinical trials may cause the development of our product candidates to be delayed.

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Even if we obtain regulatory approvals for our product candidates, the terms of approvals and ongoing regulation of our products may limit how we manufacture and market our product candidates, which could materially impair our ability to generate anticipated revenues.

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We may not meet regulatory quality standards applicable to our manufacturing and quality processes.

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Even if we receive regulatory approval to market our product candidates, the market may not be receptive to our products.

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The loss of Phillip Frost, our Chairman and Chief Executive Officer, could have a material adverse effect on our business and development.

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If we fail to attract and retain key management and scientific personnel, we may be unable to successfully develop or commercialize our product candidates.

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In the event that we successfully evolve from a company primarily involved in development to a company also involved in commercialization, we may encounter difficulties in managing our growth and expanding our operations successfully.

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If we fail to acquire and develop other products or product candidates, at all or on commercially reasonable terms, we may be unable to diversify or grow our business.

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We have no experience manufacturing our pharmaceutical product candidates other than at our Israeli and Mexican facilities and we therefore rely on third parties to manufacture and supply our pharmaceutical product candidates, and would need to meet various standards necessary to satisfy FDA regulations if and when we commence manufacturing.

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We currently have no pharmaceutical or diagnostic marketing, sales or distribution capabilities other than in Chile and Mexico for sales in those countries and our API business in Israel. If we are unable to develop our sales and marketing and distribution capability on our own or through collaborations with marketing partners, we will not be successful in commercializing our pharmaceutical product candidates.

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Independent clinical investigators and contract research organizations that we engage to conduct our clinical trials may not be diligent, careful or timely.

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The success of our business is dependent on the actions of our collaborative partners.

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Our license agreement with TESARO, Inc. is important to our business. If TESARO does not successfully develop and commercialize rolapitant, our business could be adversely affected.

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If we are unable to obtain and enforce patent protection for our products, our business could be materially harmed.

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We do not have an exclusive arrangement in place with Dr.ÌýTom Kodadek with respect to technology or intellectual property that may be material to our business.

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If we are unable to protect the confidentiality of our proprietary information and know-how, the value of our technology and products could be adversely affected.

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We rely heavily on licenses from third parties.

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We license patent rights to certain of our technology from third-party owners. If such owners do not properly maintain or enforce the patents underlying such licenses, our competitive position and business prospects will be harmed.

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Our commercial success depends significantly on our ability to operate without infringing the patents and other proprietary rights of third parties.

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Adverse results in material litigation matters or governmental inquiries could have a material adverse effect upon our business and financial condition.

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Medicare prescription drug coverage legislation and future legislative or regulatory reform of the health care system may affect our ability to sell our products profitably.

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Failure to obtain regulatory approval outside the United States will prevent us from marketing our product candidates abroad.

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We may not have the funding available to pursue acquisitions.

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Acquisitions may disrupt our business, distract our management and may not proceed as planned; and we may encounter difficulties in integrating acquired businesses.

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Non-U.S. governments often impose strict price controls, which may adversely affect our future profitability.

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Political, economic, and military instability in Israel could adversely impact our operations.

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Our business may become subject to legal, economic, political, regulatory and other risks associated with international operations.

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The market price of our common stock may fluctuate significantly.

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Directors, executive officers, principal stockholders and affiliated entities own a significant percentage of our capital stock, and they may make decisions that you do not consider to be in your best interests or in the best interests of our stockholders.

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Compliance with changing regulations concerning corporate governance and public disclosure may result in additional expenses.

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If we are unable to satisfy the requirements of SectionÌý404 of the Sarbanes-Oxley Act of 2002, as they apply to us, or our internal controls over financial reporting are not effective, the reliability of our financial statements may be questioned and our common stock price may suffer.

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We may be unable to maintain our listing on the NYSE, which could cause our stock price to fall and decrease the liquidity of our common stock.

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Future issuances of common stock and hedging activities may depress the trading price of our common stock.

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Provisions in our charter documents and Delaware law could discourage an acquisition of us by a third party, even if the acquisition would be favorable to you.

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We do not intend to pay cash dividends on our common stock in the foreseeable future.

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PART I. FINANCIAL INFORMATION

Unless the context otherwise requires, all references in this Quarterly Report on Form 10-Q to the “Company”, “СÖíÊÓƵapp”, “we”, “our”, “ours”, and “us” refer to СÖíÊÓƵapp Health, Inc., a Delaware corporation, including our wholly-owned subsidiaries.

ItemÌý 1. Financial Statements

СÖíÊÓƵapp Health, Inc. and Subsidiaries

CONDENSED CONSOLIDATED BALANCE SHEETS

(unaudited) (in thousands except share and per share data)

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Ìý ÌýÌý MarchÌý31,Ìý2012 Ìý Ìý DecemberÌý31,Ìý2011 Ìý

ASSETS

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Current assets

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Cash and cash equivalents

ÌýÌý $ 47,118 ÌýÌý Ìý $ 71,516 ÌýÌý

Marketable securities

ÌýÌý Ìý 14,997 ÌýÌý Ìý Ìý —ÌýÌý ÌýÌý

Accounts receivable, net

ÌýÌý Ìý 16,249 ÌýÌý Ìý Ìý 12,544 ÌýÌý

Inventory, net

ÌýÌý Ìý 18,393 ÌýÌý Ìý Ìý 13,339 ÌýÌý

Prepaid expenses and other current assets

ÌýÌý Ìý 2,654 ÌýÌý Ìý Ìý 2,179 ÌýÌý

Current assets of discontinued operations

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý 4 ÌýÌý
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Ìý Ìý

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Total current assets

ÌýÌý Ìý 99,411 ÌýÌý Ìý Ìý 99,582 ÌýÌý

Property and equipment, net

ÌýÌý Ìý 5,343 ÌýÌý Ìý Ìý 5,358 ÌýÌý

Intangible assets, net

ÌýÌý Ìý 75,094 ÌýÌý Ìý Ìý 76,730 ÌýÌý

Goodwill

ÌýÌý Ìý 40,319 ÌýÌý Ìý Ìý 39,815 ÌýÌý

Investments, net

ÌýÌý Ìý 10,136 ÌýÌý Ìý Ìý 6,717 ÌýÌý

Other assets

ÌýÌý Ìý 1,267 ÌýÌý Ìý Ìý 1,287 ÌýÌý
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Ìý

Ìý Ìý

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Ìý

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Total assets

ÌýÌý $ 231,570 ÌýÌý Ìý $ 229,489 ÌýÌý
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Ìý Ìý

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LIABILITIES, SERIES D PREFERRED STOCK, AND SHAREHOLDERSÂ’ EQUITY

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Current liabilities

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Accounts payable

ÌýÌý $ 4,877 ÌýÌý Ìý $ 4,891 ÌýÌý

Accrued expenses

ÌýÌý Ìý 10,389 ÌýÌý Ìý Ìý 4,956 ÌýÌý

Current portion of lines of credit and notes payable

ÌýÌý Ìý 14,194 ÌýÌý Ìý Ìý 8,757 ÌýÌý

Current liabilities of discontinued operations

ÌýÌý Ìý 245 ÌýÌý Ìý Ìý 174 ÌýÌý
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Total current liabilities

ÌýÌý Ìý 29,705 ÌýÌý Ìý Ìý 18,778 ÌýÌý

Other long-term liabilities, principally contingent consideration and deferred tax liabilities

ÌýÌý Ìý 22,499 ÌýÌý Ìý Ìý 25,443 ÌýÌý
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Ìý Ìý

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Total liabilities

ÌýÌý Ìý 52,204 ÌýÌý Ìý Ìý 44,221 ÌýÌý

Commitments and contingencies

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Series D preferred stock – $0.01 par value, 2,000,000 shares authorized; 1,129,032 and 1,129,032 shares issued and outstanding (liquidation value of $28,915 and $28,355) at MarchÌý31, 2012 and DecemberÌý31, 2011, respectively

ÌýÌý Ìý 24,386 ÌýÌý Ìý Ìý 24,386 ÌýÌý

ShareholdersÂ’ equity

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Series A Preferred stock – $0.01 par value, 4,000,000 shares authorized; No shares issued or outstanding at MarchÌý31, 2012 and DecemberÌý31, 2011, respectively

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý —ÌýÌý ÌýÌý

Series C Preferred Stock – $0.01 par value, 500,000 shares authorized; No shares issued or outstanding at March 31, 2012 or December 31, 2011

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý —ÌýÌý ÌýÌý

Common Stock – $0.01 par value, 500,000,000 shares authorized; 297,552,819 and 297,503,033 shares issued at MarchÌý31, 2012 and DecemberÌý31, 2011, respectively

ÌýÌý Ìý 2,976 ÌýÌý Ìý Ìý 2,975 ÌýÌý

Treasury stock – 2,488,477 shares at MarchÌý31, 2012 and DecemberÌý31, 2011

ÌýÌý Ìý (8,092 )Ìý Ìý Ìý (8,092 )Ìý

Additional paid-in capital

ÌýÌý Ìý 526,023 ÌýÌý Ìý Ìý 524,814 ÌýÌý

Accumulated other comprehensive income

ÌýÌý Ìý 2,406 ÌýÌý Ìý Ìý 907 ÌýÌý

Accumulated deficit

ÌýÌý Ìý (368,333 )Ìý Ìý Ìý (359,722 )Ìý
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Ìý Ìý

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Total shareholdersÂ’ equity

ÌýÌý Ìý 154,980 ÌýÌý Ìý Ìý 160,882 ÌýÌý
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Ìý Ìý

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Total liabilities, Series D Preferred Stock, and shareholdersÂ’ equity

ÌýÌý $ 231,570 ÌýÌý Ìý $ 229,489 ÌýÌý
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The accompanying Notes to Condensed Consolidated Financial Statements are an integral part of these statements.

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СÖíÊÓƵapp Health, Inc. and Subsidiaries

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

(unaudited)

(in thousands, except share and per share data)

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Ìý ÌýÌý ForÌýtheÌýthreeÌýmonthsÌýendedÌýMarchÌý31, Ìý
Ìý ÌýÌý 2012 Ìý Ìý 2011 Ìý

Revenue

ÌýÌý Ìý

Product sales

ÌýÌý $ 8,639 ÌýÌý Ìý $ 6,950 ÌýÌý

Other revenue

ÌýÌý Ìý 138 ÌýÌý Ìý Ìý —ÌýÌý ÌýÌý
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Ìý

Ìý

Ìý Ìý

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Total revenue

ÌýÌý Ìý 8,777 ÌýÌý Ìý Ìý 6,950 ÌýÌý

Cost of goods sold, excluding amortization of intangible assets

ÌýÌý Ìý 4,987 ÌýÌý Ìý Ìý 4,178 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

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Gross margin, excluding amortization of intangible assets

ÌýÌý Ìý 3,790 ÌýÌý Ìý Ìý 2,772 ÌýÌý

Operating expenses

ÌýÌý Ìý

Selling, general and administrative

ÌýÌý Ìý 4,671 ÌýÌý Ìý Ìý 5,055 ÌýÌý

Research and development

ÌýÌý Ìý 4,831 ÌýÌý Ìý Ìý 1,088 ÌýÌý

Contingent consideration

ÌýÌý Ìý 1,144 ÌýÌý Ìý Ìý —ÌýÌý ÌýÌý

Other operating expenses, principally amortization of intangible assets

ÌýÌý Ìý 1,991 ÌýÌý Ìý Ìý 765 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Total operating expenses

ÌýÌý Ìý 12,637 ÌýÌý Ìý Ìý 6,908 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Operating loss from continuing operations

ÌýÌý Ìý (8,847 )Ìý Ìý Ìý (4,136 )Ìý

Other income and (expense)

ÌýÌý Ìý

Interest income

ÌýÌý Ìý 27 ÌýÌý Ìý Ìý 8 ÌýÌý

Interest expense

ÌýÌý Ìý (351 )Ìý Ìý Ìý (87 )Ìý

Other income, net

ÌýÌý Ìý 1,298 ÌýÌý Ìý Ìý 122 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Other income and (expense), net

ÌýÌý Ìý 974 ÌýÌý Ìý Ìý 43 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Loss from continuing operations before income taxes and investment losses

ÌýÌý Ìý (7,873 )Ìý Ìý Ìý (4,093 )Ìý

Income tax provision

ÌýÌý Ìý 215 ÌýÌý Ìý Ìý 233 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Loss from continuing operations before investment losses

ÌýÌý Ìý (8,088 )Ìý Ìý Ìý (4,326 )Ìý

Loss from investments in investees

ÌýÌý Ìý (523 )Ìý Ìý Ìý (423 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Loss from continuing operations

ÌýÌý Ìý (8,611 )Ìý Ìý Ìý (4,749 )Ìý

Loss from discontinued operations, net of tax

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý (955 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Net loss

ÌýÌý Ìý (8,611 )Ìý Ìý Ìý (5,704 )Ìý

Preferred stock dividend

ÌýÌý Ìý (560 )Ìý Ìý Ìý (645 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Net loss attributable to common shareholders

ÌýÌý $ (9,171 )Ìý Ìý $ (6,349 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Loss per share, basic and diluted

ÌýÌý Ìý

Loss from continuing operations

ÌýÌý $ (0.03 )Ìý Ìý $ (0.02 )Ìý

Loss from discontinued operations

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý (0.00 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Net loss per share

ÌýÌý $ (0.03 )Ìý Ìý $ (0.02 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Weighted average number of common shares outstanding, basic and diluted

ÌýÌý Ìý 297,543,066 ÌýÌý Ìý Ìý 261,042,274 ÌýÌý

The accompanying Notes to Condensed Consolidated Financial Statements are an integral part of these statements.

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СÖíÊÓƵapp Health, Inc. and Subsidiaries

CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS

(unaudited)

(in thousands)

Ìý

Ìý ÌýÌý ForÌýtheÌýthreeÌýmonthsÌýendedÌýMarchÌý31, Ìý
Ìý ÌýÌý 2012 Ìý Ìý 2011 Ìý

Net loss attributable to common shareholders

ÌýÌý $ (9,171 )Ìý Ìý $ (6,349 )Ìý

Other comprehensive income (loss)

ÌýÌý Ìý

Change in foreign currency translation adjustment

ÌýÌý Ìý 1,390 ÌýÌý Ìý Ìý (497 )Ìý

Available for sale investments:

ÌýÌý Ìý

Change in other net unrealized gains

ÌýÌý Ìý 109 ÌýÌý Ìý Ìý —ÌýÌý ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Comprehensive loss

ÌýÌý $ (7,672 )Ìý Ìý $ (6,846 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Ìý

The accompanying Notes to Condensed Consolidated Financial Statements are an integral part of these statements.

Ìý

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СÖíÊÓƵapp Health, Inc. and Subsidiaries

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

(unaudited)

(in thousands)

Ìý

Ìý ÌýÌý ForÌýtheÌýthreeÌýmonthsÌýended
MarchÌý31,
Ìý
Ìý ÌýÌý 2012 Ìý Ìý 2011 Ìý

Cash flows from operating activities

ÌýÌý Ìý

Net loss

ÌýÌý $ (8,611 )Ìý Ìý $ (5,704 )Ìý

Loss from discontinued operations, net of tax

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý 955 ÌýÌý

Adjustments to reconcile net loss to net cash used in operating activities:

ÌýÌý Ìý

Depreciation and amortization

ÌýÌý Ìý 2,328 ÌýÌý Ìý Ìý 869 ÌýÌý

Accretion of debt discount related to notes payable

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý 2 ÌýÌý

Equity-based compensation – employees and non-employees

ÌýÌý Ìý 1,180 ÌýÌý Ìý Ìý 1,646 ÌýÌý

Loss from investments in investees

ÌýÌý Ìý 523 ÌýÌý Ìý Ìý 423 ÌýÌý

(Recovery of) provision for bad debt

ÌýÌý Ìý (151 )Ìý Ìý Ìý 17 ÌýÌý

Provision for inventory reserves

ÌýÌý Ìý 255 ÌýÌý Ìý Ìý 52 ÌýÌý

Revenue from receipt of equity

ÌýÌý Ìý (51 )Ìý Ìý Ìý —ÌýÌý ÌýÌý

Unrealized gain from warrants

ÌýÌý Ìý (1,117 )Ìý Ìý Ìý —ÌýÌý ÌýÌý

Contingent consideration

ÌýÌý Ìý 1,144 ÌýÌý Ìý Ìý —ÌýÌý ÌýÌý

Changes in assets and liabilities of continuing operations, net of the effects of acquisitions:

ÌýÌý Ìý

Accounts receivable

ÌýÌý Ìý (2,691 )Ìý Ìý Ìý (523 )Ìý

Inventory

ÌýÌý Ìý (4,433 )Ìý Ìý Ìý 1,682 ÌýÌý

Prepaid expenses and other current assets

ÌýÌý Ìý (481 )Ìý Ìý Ìý (109 )Ìý

Other assets

ÌýÌý Ìý 7 ÌýÌý Ìý Ìý 80 ÌýÌý

Accounts payable

ÌýÌý Ìý (271 )Ìý Ìý Ìý (2,149 )Ìý

Foreign currency measurement

ÌýÌý Ìý (458 )Ìý Ìý Ìý —ÌýÌý ÌýÌý

Accrued expenses

ÌýÌý Ìý 1,253 ÌýÌý Ìý Ìý (340 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Cash used in operating activities of continuing operations

ÌýÌý Ìý (11,574 )Ìý Ìý Ìý (3,099 )Ìý

Cash provided by (used in) operating activities of discontinued operations

ÌýÌý Ìý 75 ÌýÌý Ìý Ìý (1,586 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Net cash used in operating activities

ÌýÌý Ìý (11,499 )Ìý Ìý Ìý (4,685 )Ìý

Cash flows from investing activities

ÌýÌý Ìý

Acquisition of businesses, net of cash

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý (10,538 )Ìý

Purchase of marketable securities

ÌýÌý Ìý (14,997 )Ìý Ìý Ìý (59,983 )Ìý

Investments in investees

ÌýÌý Ìý (2,700 )Ìý Ìý Ìý —ÌýÌý ÌýÌý

Capital expenditures

ÌýÌý Ìý (175 )Ìý Ìý Ìý (108 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Net cash used in investing activities

ÌýÌý Ìý (17,872 )Ìý Ìý Ìý (70,629 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Cash flows from financing activities:

ÌýÌý Ìý

Issuance of common stock, including related parties, net

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý 104,828 ÌýÌý

Borrowing under lines of credit

ÌýÌý Ìý 10,337 ÌýÌý Ìý Ìý 3,027 ÌýÌý

Repayments under lines of credit

ÌýÌý Ìý (5,490 )Ìý Ìý Ìý (2,827 )Ìý

Proceeds from the exercise of stock options and warrants

ÌýÌý Ìý 31 ÌýÌý Ìý Ìý 135 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Net cash provided by financing activities

ÌýÌý Ìý 4,878 ÌýÌý Ìý Ìý 105,163 ÌýÌý

Effect of exchange rate changes on cash and cash equivalents

ÌýÌý Ìý 95 ÌýÌý Ìý Ìý 14 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Net (decrease) increase in cash and cash equivalents

ÌýÌý Ìý (24,398 )Ìý Ìý Ìý 29,863 ÌýÌý

Cash and cash equivalents at beginning of period

ÌýÌý Ìý 71,516 ÌýÌý Ìý Ìý 18,016 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Cash and cash equivalents at end of period

ÌýÌý $ 47,118 ÌýÌý Ìý $ 47,879 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

SUPPLEMENTAL INFORMATION

ÌýÌý Ìý

Interest paid

ÌýÌý $ 177 ÌýÌý Ìý $ 65 ÌýÌý

Income taxes refunded

ÌýÌý $ (6 )Ìý Ìý $ —ÌýÌý ÌýÌý

Ìý

The accompanying Notes to Condensed Consolidated Financial Statements are an integral part of these statements.

Ìý

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СÖíÊÓƵapp Health, Inc. and Subsidiaries

NOTES TO CONDENSED CONSOLIDATED FINANCIAL STATEMENTS (unaudited)

NOTE 1 BUSINESS AND ORGANIZATION

We are a multi-national pharmaceutical and diagnostics company that seeks to establish industry-leading positions in large and rapidly growing medical markets by leveraging our discovery, development and commercialization expertise and our novel and proprietary technologies. We are developing a range of solutions to diagnose, treat and prevent various conditions, including molecular diagnostics tests, point-of-care tests, and proprietary pharmaceuticals and vaccines. We plan to commercialize these solutions on a global basis in large and high growth markets, including emerging markets. We have already established emerging markets pharmaceutical platforms in Chile and Mexico, which are generating revenue and which we expect to generate positive cash flow and facilitate future market entry for our products currently in development. We also operate a specialty active pharmaceutical ingredients (“APIs”) manufacturer in Israel, which is currently generating revenue and positive cash flow, and which we expect to play a valuable role in the development of our pipeline of peptoids and other molecules for our proprietary molecular diagnostic and therapeutic products. We continue to actively explore opportunities to acquire complementary pharmaceuticals, compounds, technologies, and businesses.

We are incorporated in Delaware and our principal executive offices are located in Miami, Florida. We lease office and lab space in Jupiter and Miramar, Florida, which is where our molecular diagnostics research and development and oligonucleotide research and development operations are based, respectively. We lease office, manufacturing, research and development and warehouse space in Woburn, Massachusetts for our point-of-care diagnostics business, and in Nesher, Israel for our API business. Our Chilean operations are located in leased offices and a leased warehouse facility in Santiago, Chile, and we own an office and manufacturing facility, and lease a warehouse facility in Guadalajara, Mexico.

NOTE 2 SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES

Basis of presentation. The accompanying unaudited interim condensed consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States and with the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, they do not include all information and notes required by accounting principles generally accepted in the United States for complete financial statements. In the opinion of management, all adjustments (consisting of only normal recurring adjustments) considered necessary to present fairly the CompanyÂ’s results of operations, financial position and cash flows have been made. The results of operations and cash flows for the three months ended MarchÌý31, 2012, are not necessarily indicative of the results of operations and cash flows that may be reported for the remainder of 2012 or for future periods. The unaudited condensed consolidated financial statements should be read in conjunction with the Consolidated Financial Statements and the Notes to Consolidated Financial Statements included in our Annual Report on Form 10-K for the year ended DecemberÌý31, 2011.

Reclassifications. As further discussed in Note 6, the results of operations and the assets and the liabilities related to the Instrumentation Business have been accounted for as discontinued operations. Accordingly, the results of the operations related to the Instrumentation Business from prior periods have been reclassified to discontinued operations.

We have reclassified certain expenses previously recorded in selling, general and administrative expenses to inventory as of MarchÌý31, 2012. This reclassification resulted in a reduction of cost of goods sold of $0.4 million ($0.00 per share). The activities reclassified were primarily related to certain costs related to the procurement of inventory at our Chilean pharmaceutical business.

Principles of consolidation. The accompanying unaudited condensed consolidated financial statements include the accounts of СÖíÊÓƵapp Health, Inc. and our wholly-owned subsidiaries. All significant intercompany accounts and transactions are eliminated in consolidation.

Use of estimates. The preparation of financial statements in conformity with accounting principles generally accepted in the United States of America requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and expenses during the reporting period. Actual results could differ from those estimates.

Ìý

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Cash and cash equivalents. Cash and cash equivalents consist of short-term, interest-bearing instruments with original maturities of 90 days or less at the date of purchase. We also consider all highly liquid investments with original maturities at the date of purchase of 90 days or less as cash equivalents. These investments include money markets, bank deposits, and U.S. treasury securities.

Marketable securities. Investments with original maturities of greater than 90 days and remaining maturities of less than one year are classified as marketable securities. Marketable securities include U.S. treasury securities. Unrealized gains and temporary losses on investments are included in accumulated other comprehensive income (loss) as a separate component of stockholdersÂ’ equity. Realized gains and losses, dividends, interest income, and declines in value judged to be other-than-temporary credit losses are included in other income (expense). Amortization of any premium or discount arising at purchase is included in interest income.

Comprehensive loss. Our comprehensive loss for the three months ended MarchÌý31, 2012 includes (i) the net loss for the three months, (ii) the unrealized gain of $0.1 million on our common stock options and warrants of Neovasc, Inc. (“Neovasc”) (Refer to Note 5), and (iii) the cumulative translation adjustment, net, of $1.4 million for the translation results of our subsidiaries in Chile and Mexico. Comprehensive loss for the three months ended MarchÌý31, 2011 includes net loss for the three months and the cumulative translation adjustment, net, of $0.5 million for the translation results of our subsidiaries in Chile and Mexico.

Revenue recognition. Generally, we recognize revenue from product sales when goods are shipped and title and risk of loss transfer to our customers.

Other revenue includes revenue related to upfront license payments, license fees and milestone payments received through our license, collaboration and commercialization agreements. We analyze our multiple-element arrangements to determine whether the elements can be separated and accounted for individually as separate units of accounting. In addition, other revenue includes $0.1 million of revenue related to our consulting agreement we entered into with Neovasc. Refer to Note 5. We recognize the revenue on a straight-line basis over the contractual term of the agreement.

Non-refundable license fees for the out-license of our technology are recognized depending on the provisions of each agreement. We recognize non-refundable upfront license payments as revenue upon receipt if the license has standalone value and the fair value of our undelivered obligations, if any, can be determined. If the license is considered to have standalone value but the fair value of any of the undelivered items cannot be determined, the license payments are recognized as revenue over the period of our performance for such undelivered items or services. License fees with ongoing involvement or performance obligations are recorded as deferred revenue once received and generally are recognized ratably over the period of such performance obligation only after both the license period has commenced and we have delivered the technology. Our assessment of our obligations and related performance periods requires significant management judgment. If an agreement contains research and development obligations, the relevant time period for the research and development phase is based on management estimates and could vary depending on the outcome of clinical trials and the regulatory approval process. Such changes could materially impact the revenue recognized, and as a result, management reviews the estimates related to the relevant time period of research and development on a quarterly basis.

Revenue from milestone payments related to arrangements under which we have continuing performance obligations are recognized as revenue upon achievement of the milestone only if all of the following conditions are met: the milestone payments are non-refundable; there was substantive uncertainty at the date of entering into the arrangement that the milestone would be achieved; the milestone is commensurate with either the vendorÂ’s performance to achieve the milestone or the enhancement of the value of the delivered item by the vendor; the milestone relates solely to past performance; and the amount of the milestone is reasonable in relation to the effort expended or the risk associated with the achievement of the milestone. If any of these conditions are not met, the milestone payments are not considered to be substantive and are, therefore, deferred and recognized as revenue over the term of the arrangement as we complete our performance obligations.

Total deferred revenue related to other revenues was $1.8 million and $0.9 million at MarchÌý31, 2012 and DecemberÌý31, 2011, respectively.

Ìý

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Derivative financial instruments. We record derivative financial instruments on our balance sheet at their fair value and the changes in the fair value are recognized in income when they occur, the only exception being derivatives that qualify as hedges. To qualify the derivative instrument as a hedge, we are required to meet strict hedge effectiveness and contemporaneous documentation requirements at the initiation of the hedge and assess the hedge effectiveness on an ongoing basis over the life of the hedge. At MarchÌý31, 2012 and DecemberÌý31, 2011, our forward contracts for inventory purchases did not meet the documentation requirements to be designated as hedges. Accordingly, we recognize all changes in fair values in income. Refer to Note 7.

Product warranties. Product warranty expense is recorded concurrently with the recording of revenue for product sales. The costs of warranties are accounted for as a component of cost of sales. We estimate warranty costs based on our estimated historical experience and adjust for any known product reliability issues.

Allowance for doubtful accounts. We analyze accounts receivable and historical bad debt levels, customer credit worthiness and current economic trends when evaluating the adequacy of the allowance for doubtful accounts using the specific identification method. Our reported net loss is directly affected by our estimate of the collectability of accounts receivable. Estimated allowances for sales returns are based upon our history of product returns. The amount of allowance for doubtful accounts was $0.3 million and $0.4 million at MarchÌý31, 2012 and DecemberÌý31, 2011, respectively.

Segment reporting. Our chief operating decision-maker (“CODM”) is comprised of our executive management with the oversight of our board of directors. Our CODM reviews our operating results and operating plans and make resource allocation decisions on a company-wide or aggregate basis. We currently manage our operations in one reportable segment, pharmaceutical. The pharmaceutical segment consists of two operating segments, our (i)Ìýpharmaceutical research and development segment which is focused on the research and development of pharmaceutical products, diagnostic tests and vaccines, and (ii)Ìýthe pharmaceutical operations we acquired in Chile, Mexico and Israel through the acquisition of СÖíÊÓƵapp Chile, Exakta-СÖíÊÓƵapp and FineTech Pharmaceuticals, respectively. There are no inter-segment sales. We evaluate the performance of each operating segment based on operating profit or loss. There is no inter-segment allocation of interest expense and income taxes.

Equity-based compensation. We measure the cost of employee services received in exchange for an award of equity instruments based on the grant-date fair value of the award. That cost is recognized in the statement of operations over the period during which an employee is required to provide service in exchange for the award. We record excess tax benefits, realized from the exercise of stock options as a financing cash inflow rather than as a reduction of taxes paid in cash flow from operations. Equity-based compensation arrangements to non-employees are recorded at their fair value on the measurement date. The measurement of equity-based compensation is subject to periodic adjustment as the underlying equity instruments vest. During the three months ended MarchÌý31, 2012 and 2011, we recorded $1.2 million and $1.6 million, respectively, of equity-based compensation expense.

Recent accounting pronouncements. On JanuaryÌý1, 2012, we adopted an amendment issued by the Financial Accounting Standards Board (“FASB”) to the accounting standards related to fair value measurements and disclosure requirements. This standard provides certain amendments to the existing guidance on the use and application of fair value measurements and maintains a definition of fair value that is based on the notion of exit price. The adoption of this standard did not have a material impact on our consolidated financial statements.

On JanuaryÌý1, 2012, we adopted amendments issued by the FASB to the accounting standards related to the presentation of comprehensive income. These standards revise the manner in which entities present comprehensive income in their financial statements and remove the option to present items of other comprehensive income in the statement of changes in stockholdersÂ’ equity. These standards require an entity to report components of comprehensive income in either (1)Ìýa continuous statement of comprehensive income, or (2)Ìýtwo separate but consecutive statements of net income and other comprehensive income. We modified our financial statements presentation using the latter alternative.

On JanuaryÌý1, 2012, we adopted revised guidance issued by the FASB related to the testing of goodwill for impairment. Under the revised guidance, an entity has the option to perform a qualitative assessment of whether it is more-likely-than-not that a reporting unitÂ’s fair value is less than its carrying value prior to performing the two-step quantitative goodwill impairment test. If, based on the qualitative factors, an entity determines that the fair value of the reporting unit is greater than its carrying amount, then the entity would not be required to perform the two-step quantitative impairment test for that reporting unit. However, if the qualitative assessment indicates that it is not more-likely-than-not that the reporting unitÂ’s fair value exceeds its carrying value, then the quantitative assessment

Ìý

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must be performed. An entity is permitted to perform the qualitative assessment on none, some or all of its reporting units and may also elect to bypass the qualitative assessment and begin with the quantitative assessment of goodwill impairment. This amendment did not have a material impact on our consolidated financial statements.

NOTE 3 LOSS PER SHARE

Basic loss per share is computed by dividing our net loss by the weighted average number of shares outstanding during the period. Diluted earnings per share is computed by dividing our net loss by the weighted average number of shares outstanding and the impact of all dilutive potential common shares, primarily stock options. The dilutive impact of stock options and warrants is determined by applying the “treasury stock” method.

A total of 27,416,029 and 27,604,138 potential common shares have been excluded from the calculation of net loss per share for the three months ended MarchÌý31, 2012 and 2011, respectively, because their inclusion would be anti-dilutive. As of MarchÌý31, 2012, the holders of our Series D Preferred Stock could convert their Preferred Shares into approximately 11,659,137 shares of our Common Stock.

NOTE 4 COMPOSITION OF CERTAIN FINANCIAL STATEMENT CAPTIONS

Ìý

(in thousands)

ÌýÌý MarchÌý31,
2012
Ìý Ìý DecemberÌý31,
2011
Ìý

Accounts receivable, net:

ÌýÌý Ìý

Accounts receivable

ÌýÌý $ 16,573 ÌýÌý Ìý $ 12,984 ÌýÌý

Less allowance for doubtful accounts

ÌýÌý Ìý (324 )Ìý Ìý Ìý (440 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý
ÌýÌý $ 16,249 ÌýÌý Ìý $ 12,544 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Inventories, net:

ÌýÌý Ìý

Finished products

ÌýÌý $ 16,247 ÌýÌý Ìý $ 11,100 ÌýÌý

Work-in process

ÌýÌý Ìý 505 ÌýÌý Ìý Ìý 277 ÌýÌý

Raw materials

ÌýÌý Ìý 2,245 ÌýÌý Ìý Ìý 2,287 ÌýÌý

Less inventory reserve

ÌýÌý Ìý (604 )Ìý Ìý Ìý (325 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý
ÌýÌý $ 18,393 ÌýÌý Ìý $ 13,339 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Intangible assets, net:

ÌýÌý Ìý

Customer relationships

ÌýÌý $ 18,654 ÌýÌý Ìý $ 18,386 ÌýÌý

In-process research and development

ÌýÌý Ìý 10,000 ÌýÌý Ìý Ìý 10,000 ÌýÌý

Technology

ÌýÌý Ìý 47,100 ÌýÌý Ìý Ìý 47,100 ÌýÌý

Product registrations

ÌýÌý Ìý 4,154 ÌýÌý Ìý Ìý 3,895 ÌýÌý

Tradename

ÌýÌý Ìý 856 ÌýÌý Ìý Ìý 827 ÌýÌý

Covenants not to compete

ÌýÌý Ìý 1,565 ÌýÌý Ìý Ìý 1,560 ÌýÌý

Other

ÌýÌý Ìý 297 ÌýÌý Ìý Ìý 297 ÌýÌý

Less accumulated amortization

ÌýÌý Ìý (7,532 )Ìý Ìý Ìý (5,335 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý
ÌýÌý $ 75,094 ÌýÌý Ìý $ 76,730 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Other long-term obligations

ÌýÌý Ìý

Contingent consideration

ÌýÌý $ 14,804 ÌýÌý Ìý $ 18,002 ÌýÌý

Deferred tax liabilities

ÌýÌý Ìý 6,981 ÌýÌý Ìý Ìý 6,863 ÌýÌý

Other, including deferred revenue

ÌýÌý Ìý 714 ÌýÌý Ìý Ìý 578 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý
ÌýÌý $ 22,499 ÌýÌý Ìý $ 25,443 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

The change in value of the intangible assets include the foreign currency fluctuation between the Chilean and Mexican pesos against the US dollar at MarchÌý31, 2012 and DecemberÌý31, 2011.

NOTE 5 ACQUISITIONS, INVESTMENTS, AND LICENSES

FineTech acquisition

On DecemberÌý29, 2011, we purchased all of the issued and outstanding shares of FineTech Pharmaceuticals, Ltd., (“FineTech”) a privately held Israeli company focused on the development and production of specialty Active Pharmaceutical Ingredients (“APIs”). At closing, we delivered to the seller $27.7 million, of which $10.0 million

Ìý

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was paid in cash and $17.7 million was paid in shares of our common stock. The shares delivered at closing were valued at $17.7 million based on the closing sales price per share of our common stock as reported by the New York Stock Exchange (“NYSE”) on the actual closing date of the acquisition, or $4.90 per share. The number of shares issued was based on the average closing sales price per share of our common stock as reported on the NYSE for the ten trading days immediately preceding the execution of the purchase agreement, or $4.84 per share. Upon finalization of the closing financial statements of FineTech, we accrued an additional $0.5 million for a working capital surplus, as defined in the purchase agreement, which was paid to the seller in FebruaryÌý2012. In addition, the purchase agreement provides for the payment of additional cash consideration subject to the achievement of certain sales milestones.

The following table summarizes the estimated fair value of the net assets acquired and liabilities assumed in the acquisition of FineTech at the date of acquisition, which are subject to change while contingencies that existed on the acquisition date are resolved:

Ìý

(in thousands)

ÌýÌý Ìý Ìý

Current assets (including cash of $2,000)

ÌýÌý $ 3,358 ÌýÌý

Intangible assets:

ÌýÌý

Customer relationships

ÌýÌý Ìý 14,200 ÌýÌý

Technology

ÌýÌý Ìý 2,700 ÌýÌý

Non-compete

ÌýÌý Ìý 1,500 ÌýÌý

Tradename

ÌýÌý Ìý 400 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý

Total intangible assets

ÌýÌý Ìý 18,800 ÌýÌý

Goodwill

ÌýÌý Ìý 11,623 ÌýÌý

Plant and equipment

ÌýÌý Ìý 1,358 ÌýÌý

Other assets

ÌýÌý Ìý 1,154 ÌýÌý

Accounts payable and accrued expenses

ÌýÌý Ìý (910 )Ìý

Deferred tax liability

ÌýÌý Ìý (2,457 )Ìý

Contingent consideration

ÌýÌý Ìý (4,747 )Ìý
ÌýÌý

Ìý

Ìý

Ìý

Total purchase price

ÌýÌý $ 28,179 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý

Claros Diagnostics acquisition

On OctoberÌý13, 2011, we acquired Claros Diagnostics, Inc. (“Claros”) pursuant to an agreement and plan of merger. We paid $10.0 million in cash, subject to certain set-offs and deductions, and $22.5 million in shares of our common stock, based on the closing sales price per share of our common stock as reported by the NYSE on the closing date of the merger, or $5.04 per share. The number of shares issued was based on the average closing sales price per share of our common stock as reported by the NYSE for the ten trading days immediately preceding the date of the merger, or $4.45 per share. Pursuant to the merger agreement, $5.0 million of the stock consideration is held in a separate escrow account to secure the indemnification obligations of Claros under the Claros merger agreement. In DecemberÌý2011, we made a $0.2 million claim against the escrow for certain undisclosed liabilities. In addition, the merger agreement provides for the payment of up to an additional $19.125 million in shares of our common stock upon and subject to the achievement of certain milestones.

The following table summarizes the estimated fair value of the net assets acquired and liabilities assumed in the acquisition of Claros at the date of acquisition, which are subject to change while contingencies that existed on the acquisition date are resolved:

Ìý

(in thousands)

ÌýÌý Ìý Ìý

Current assets (including cash of $351)

ÌýÌý $ 378 ÌýÌý

Technology

ÌýÌý Ìý 44,400 ÌýÌý

Goodwill

ÌýÌý Ìý 17,977 ÌýÌý

Equipment

ÌýÌý Ìý 333 ÌýÌý

Other assets

ÌýÌý Ìý 18 ÌýÌý

Accounts payable and accrued expenses

ÌýÌý Ìý (655 )Ìý

Deferred tax liability

ÌýÌý Ìý (17,254 )Ìý

Contingent consideration

ÌýÌý Ìý (12,745 )Ìý
ÌýÌý

Ìý

Ìý

Ìý

Total purchase price

ÌýÌý $ 32,452 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý

Ìý

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Investments

In February 2012, we made a $1.0 million investment in ChromaDex Corporation (“ChromaDex”), a publicly traded company and leading provider of proprietary ingredients and products for the dietary supplement, nutraceutical, food and beverage, functional food, pharmaceutical and cosmetic markets, in exchange for 1,333,333 shares of ChromaDex common stock, at $0.75 per share. In connection with our investment, we also entered into a license, supply and distribution agreement with ChromaDex pursuant to which we obtained exclusive distribution rights to certain of its products in Latin America. Our investment was part of a $3.7 million private placement by Chromadex. Other investors participating in the private financing included certain related parties. Refer to Note 9.

We have determined that our ownership, along with our related parties do not provide us with significant influence over the operations of ChromaDex and as a result, we account for ChromaDex under the cost method.

In February 2012, we purchased from Biozone Pharmaceuticals, Inc., a publicly traded company that specializes in drug development, (“BZNE”), $1.7 million of 10% secured convertible promissory notes (the “BZNE Notes”), convertible into BZNE common stock at a price equal to $0.20 per common share, which Notes are due and payable on FebruaryÌý24, 2014 and ten year warrants (the “BZNE Warrants”) to purchase 8.5Ìýmillion shares of BZNE common stock at an exercise price of $0.40 per share. The Notes are secured pursuant to a security agreement by a first priority lien in the assets of BZNE, including the stock of its subsidiaries. As further consideration for the purchase of the Notes by us, BZNE granted us exclusive, worldwide distribution rights to its enhanced formulation of propofol. The parties also entered into a license agreement pursuant to which we acquired a world-wide license for the development and commercialization of products utilizing BZNEÂ’s proprietary drug delivery technology, including QuSomes, exclusively for СÖíÊÓƵapp in the field of ophthalmology and non-exclusive for all other therapeutic fields, subject in each case to certain excluded products. Refer to Note 9.

We have accounted for the BZNE Notes as an available for sale investment. We recorded the BZNE Notes and BZNE Warrants at fair value on the date of acquisition, initially valuing the BZNE Notes at $1.7 million and the BZNE Warrants at $1.1 million, which was recorded in other income and expense, net. As a result, we recorded the investment at a total of $2.8 million. Changes in fair value for the BZNE Notes will be recorded through other comprehensive income each reporting period and changes in fair value for the beneficial conversion feature of the BZNE Notes and the BNZE Warrants will be recorded in other income and expense in our Statement of Operations. The trading activity in BZNE does not represent an active market and as such, we have determined the fair market value utilizing a business enterprise valuation approach in order to determine the fair value of our investment in BZNE.

We have determined that BZNE has an insufficient amount of equity to carry out its principal activities without additional financial support and meets the definition of a variable interest entity (“VIE”). We determined that we do not have the power to direct the activities of BZNE which most significantly impact its economic performance and as such, have determined that we are not the primary beneficiary of BZNE. We will continue to evaluate our relationship with BZNE including if we convert the BZNE Notes or BZNE Warrants into BZNE common stock.

In AugustÌý2011, we made an investment in Neovasc, a medical technology company that is publicly traded in Canada and based in Vancouver, Canada. Neovasc is developing devices to treat cardiovascular diseases and is also a leading supplier of tissue components for the manufacturers of replacement heart valves. We invested $2.0 million and received two million Neovasc common shares, and two-year warrants to purchase an additional one million shares for $1.25 a share. We recorded the warrants on the date of grant at their estimated fair value of $0.7 million using the Black-Scholes-Merton Model. Prior to the warrants being readily convertible into cash, we recorded an unrealized gain of $0.2 million in other comprehensive income. During the three months ended March, 31, 2012 we recorded an unrealized gain of $0.1 million related to these warrants to reflect the increase in the closing price of Neovasc common stock in other income and expense, net. We also entered into an agreement with Neovasc to provide strategic advisory services to Neovasc as it continues to develop and commercialize its novel cardiac devices. In connection with the consulting agreement, Neovasc granted us 913,750 common stock options. The options were granted at (Canadian) $1.00 per share and vest annually over three years. We valued the options using the Black-Scholes-Merton Model at $0.8 million on the date of grant and will recognize the revenue over four years as other revenue. Through MarchÌý31, 2012, we have recorded other comprehensive income of $0.3 million including $0.1 million during the three months ended MarchÌý31, 2012. The unrealized gain reflects the increase in share price of Neovasc to the (Canadian) $1.40. Refer to Note 9.

In December 2010, we entered into a license agreement (the “TESARO License”) with TESARO, Inc. (“TESARO”) granting TESARO exclusive rights to the development, manufacture, commercialization and distribution of rolapitant and a related compound. In connection with the TESARO License, we also acquired an equity position in TESARO. We recorded the equity position at $0.7 million, the estimated fair value based on a discounted cash flow model.

Neither we nor our related parties have the ability to significantly influence TESARO and as such, we account for our investment in TESARO under the cost method. In JuneÌý2011, TESARO announced a $101 million financing. In connection with that financing, we determined TESARO no longer meets the definition of a variable interest entity as it has sufficient capital to carry out its principal activities without additional financial support.

In NovemberÌý2010, we made an investment in Fabrus, Inc., a privately held early stage biotechnology company with next generation therapeutic antibody drug discovery and development capabilities. Fabrus is using its proprietary antibody screening and engineering approach to discover promising lead compounds against several important oncology targets. Our investment was part of a $2.1Ìýmillion financing for Fabrus and included other related parties. Refer to Note 9.

Ìý

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Table of Contents

In SeptemberÌý2009, we entered into an agreement pursuant to which we invested $2.5 million in cash in Cocrystal Discovery, Inc., a privately held biopharmaceutical company (“Cocrystal”) in exchange for 1,701,723 shares of CocrystalÂ’s Convertible SeriesÌýA Preferred Stock. Cocrystal is focused on the discovery and development of novel antiviral drugs using a combination of protein structure-based approaches. Refer to Note 9.

In OctoberÌý2011, Cocrystal received an investment of $7.5 million from Teva Pharmaceutical Industries Ltd. In connection with that investment, we determined Cocrystal no longer meets the definition of a variable interest entity as it has sufficient capital to carry out its principal activities without additional financial support. As a result of the CompanyÂ’s and its related partiesÂ’ ownership interest, the Company and its related parties have the ability to significantly influence Cocrystal, and we account for our investment under the equity method.

In JuneÌý2009, we entered into a stock purchase agreement with Sorrento Therapeutics, Inc. (“Sorrento”), a publicly held company with a technology for generating fully human monoclonal antibodies, pursuant to which we invested $2.3Ìýmillion in Sorrento. The closing stock price for SorrentoÂ’s common stock, a thinly traded stock, as quoted on the over-the-counter markets was $0.59 per share on MarchÌý31, 2012. Refer to Note 9.

Variable interest entities

We have determined that we hold a variable interests in two entities, Fabrus and BZNE. We made this determination as a result of our assessment that they do not have sufficient resources to carry out their principal activities without additional financial support.

In order to determine the primary beneficiary of Fabrus, we evaluated our investment and our related parties’ investments, as well as our investment combined with the related party group’s investment to identify if we had the power to direct the activities that most significantly impact the economic performance of Fabrus. The related party group when considering our investment in Fabrus includes the Company, Frost Gamma Investments Trust, of which Phillip Frost is the sole trustee (the “Gamma Trust”), Hsu Gamma Investment, L.P., of which Jane Hsiao is the general partner (“Hsu Gamma”), and the Richard Lerner Family Trust. Drs. Frost, Hsiao and Lerner are all members of our Board of Directors. As of March 31, 2012 we own approximately 13% of Fabrus and Dr.’s Frost, Hsiao and Lerner own a total of 24% of Fabrus’ voting stock on an as converted basis, including 16% held by the Gamma Trust. Drs. Frost and Hsiao currently serve on the board of directors of Fabrus and represent 40% of its board. Based on this analysis, we determined that neither we nor our related parties have the power to direct the activities of Fabrus. However, we did determine that our related parties can significantly influence the success of Fabrus through our related parties board representation and voting power. As we have the ability to exercise significant influence over Fabrus’ operations, we account for our investments in Fabrus under the equity method.

In order to determine the primary beneficiary of BZNE, we evaluated our investment and our related partiesÂ’ investments, as well as our investment combined with the related party groupÂ’s investments to identify if we had the power to direct the activities that most significantly impact the economic performance of BZNE. We determined that power to direct the activities that most significantly impact BZNEÂ’s economic performance is conveyed through the board of directors of BZNE and no entity is able to appoint BZNEÂ’s governing body who oversee its executive management team. Based on the capital structure, governing documents and overall business operations, we determined that, while a VIE, no single entity has the power to direct the activities that most significantly impact BZNEÂ’s economic performance.

Ìý

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Table of Contents

The total assets, liabilities, and net losses of our equity method investees as of and for the three months ended MarchÌý31, 2012 were $19.7Ìýmillion, $1.6Ìýmillion, and $3.9Ìýmillion, respectively. The following table reflects our maximum exposure, accounting method, ownership interest and underlying equity in net assets of each of our investments:

Ìý

Investee name

ÌýÌý Year
invested
Ìý ÌýÌý

AccountingÌýmethod

ÌýÌý OwnershipÌýat
MarchÌý31,Ìý 2012
Ìý Ìý (inÌýthousands) Ìý Ìý Underlying
equityÌýinÌýnet
assets
Ìý

Cocrystal

ÌýÌý Ìý 2009 ÌýÌý ÌýÌý Equity method ÌýÌý Ìý 16 %Ìý Ìý $ 2,500 ÌýÌý Ìý $ 1,383 ÌýÌý

Sorrento

ÌýÌý Ìý 2009 ÌýÌý ÌýÌý Equity method ÌýÌý Ìý 23 %Ìý Ìý Ìý 2,300 ÌýÌý Ìý Ìý 765 ÌýÌý

Neovasc

ÌýÌý Ìý 2011 ÌýÌý ÌýÌý EquityÌýmethod,Ìýcost (warrants) ÌýÌý Ìý 4 %Ìý Ìý Ìý 2,013 ÌýÌý Ìý Ìý 214 ÌýÌý

ChromaDex

ÌýÌý Ìý 2012 ÌýÌý ÌýÌý Cost method ÌýÌý Ìý 2 %Ìý Ìý Ìý 1,000 ÌýÌý Ìý Ìý 125 ÌýÌý

Fabrus

ÌýÌý Ìý 2010 ÌýÌý ÌýÌý VIE, equity method ÌýÌý Ìý 13 %Ìý Ìý Ìý 650 ÌýÌý Ìý Ìý 132 ÌýÌý

TESARO

ÌýÌý Ìý 2010 ÌýÌý ÌýÌý Cost method ÌýÌý Ìý 2 %Ìý Ìý Ìý 731 ÌýÌý Ìý Ìý 1,835 ÌýÌý

Less accumulated losses in investees

ÌýÌý Ìý Ìý (3,178 )Ìý Ìý
ÌýÌý ÌýÌý ÌýÌý Ìý

Ìý

Ìý

Ìý Ìý

Total

ÌýÌý ÌýÌý ÌýÌý Ìý $ 6,016 ÌýÌý Ìý

Biozone

ÌýÌý Ìý 2012 ÌýÌý ÌýÌý

Investment available for sale

ÌýÌý Ìý N/A ÌýÌý Ìý Ìý 2,779 ÌýÌý Ìý Ìý N/A ÌýÌý

Neovasc options

ÌýÌý ÌýÌý ÌýÌý Ìý Ìý 813 ÌýÌý Ìý

Plus unrealized gain on Neovasc options and warrants

ÌýÌý Ìý Ìý 528 ÌýÌý Ìý
ÌýÌý ÌýÌý ÌýÌý Ìý

Ìý

Ìý

Ìý Ìý

TOTAL

ÌýÌý ÌýÌý ÌýÌý Ìý $ 10,136 ÌýÌý Ìý
ÌýÌý ÌýÌý ÌýÌý Ìý

Ìý

Ìý

Ìý Ìý

NOTE 6 DISCONTINUED OPERATIONS

In SeptemberÌý2011, we announced that we entered into an agreement with Optos, Inc., a subsidiary of Optos plc (collectively (“Optos”) to sell our ophthalmic instrumentation business. Upon closing in OctoberÌý2011, we received $17.5 million of cash and we will receive royalties up to $22.5 million on future sales.

The assets and liabilities related to our instrumentation business have identifiable cash flows that are independent of the cash flows of other groups of assets and liabilities and we will not have a significant continuing involvement with the related products beyond one year after the closing of the transactions. Therefore, the accompanying Condensed Consolidated Balance Sheets report the assets and liabilities related to our instrumentation business as discontinued operations in all periods presented, and the results of operations related to our instrumentation business have been classified as discontinued operations in the accompanying Condensed Consolidated Statements of Operations for all periods presented.

The following table presents the major classes of assets and liabilities that have been presented as assets of discontinued operations and liabilities of discontinued operations in the accompanying Condensed Consolidated Balance Sheets:

Ìý

(in thousands)

ÌýÌý MarchÌý31,
2012
Ìý ÌýÌý DecemberÌý31,
2011
Ìý

Trade accounts receivable, net

ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ —ÌýÌý ÌýÌý

Inventories, net

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý

Other current assets

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 4 ÌýÌý

Property, plant and equipment, net

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý

Intangible assets, net

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Total assets of discontinued operations

ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ 4 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Trade accounts payable

ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ 1 ÌýÌý

Accrued expenses and other liabilities

ÌýÌý Ìý 245 ÌýÌý ÌýÌý Ìý 173 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Total liabilities of discontinued operations

ÌýÌý $ 245 ÌýÌý ÌýÌý $ 174 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Ìý

17


Table of Contents

The following table presents summarized financial information for the discontinued operations presented in the Condensed Consolidated Statements of Operations:

Ìý

Ìý ÌýÌý ForÌýtheÌýthreeÌýmonthsÌý ended
MarchÌý31
Ìý
(in thousands) ÌýÌý 2012 Ìý ÌýÌý 2011 Ìý

Total revenue

ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ 1,698 ÌýÌý

Operating loss

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý (950 )Ìý

Loss before provision for income taxes

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý (955 )Ìý

Net loss

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý (955 )Ìý

NOTE 7 FAIR VALUE MEASUREMENTS

We record fair value at an exit price, representing the amount that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market participants. As such, fair value is a market-based measurement that should be determined based on assumptions that market participants would use in pricing an asset or liability. We utilize a three-tier fair value hierarchy, which prioritizes the inputs used in measuring fair value. These tiers include: Level 1, defined as observable inputs such as quoted prices in active markets; Level 2, defined as inputs other than quoted prices in active markets that are either directly or indirectly observable; and Level 3, defined as unobservable inputs in which little or no market data exists, therefore requiring an entity to develop its own assumptions.

As of MarchÌý31, 2012, we have money market funds that qualify as cash equivalents, U.S. Treasury securities that qualify as cash equivalents, U.S. Treasury securities recorded as marketable securities, forward contracts for inventory purchases (Refer to Note 8) and contingent consideration related to the acquisitions of CURNA, Claros and FineTech (Refer to Note 10) that are required to be measured at fair value on a recurring basis. Our U.S. Treasury securities mature on April 26, 2012 ($10.0 million) and June 28, 2012 ($15.0 million). Of the $19.1 million of contingent consideration, $4.3 million is recorded as an accrued expense and $14.8 million is recorded in other long-term liabilities. We valued the contingent consideration utilizing a discounted cash flow model for the expected payments.

In addition, in connection with our investment in Neovasc as well as entering into our consulting agreement with Neovasc, we record our options and warrants at fair value. Refer to Note 5. In connection with our BNZE investment, we recorded the BZNE Notes and BZNE Warrants at fair value on the date of acquisition, initially valuing the BZNE Notes at $1.7 million and the BZNE Warrants at $1.1 million which was recorded in other income and expense, net. As a result, we recorded the investment at a total of $2.8 million. Changes in fair value for the BZNE Notes will be recorded through other comprehensive income each reporting period and changes in fair value for the beneficial conversion feature of the BZNE Notes and the BNZE Warrants will be recorded in other income and expense in our Statement of Operations. The trading activity in BZNE does not represent an active market and as such, we have determined the fair market value utilizing a business enterprise valuation approach in order to determine the fair value of our investment in BZNE.

The carrying value of our other assets and liabilities approximates their fair value due to their short-term nature.

Any future fluctuation in fair value related to these instruments that is judged to be temporary, including any recoveries of previous write-downs, would be recorded in accumulated other comprehensive income or loss. If we determine that any future valuation adjustment was other-than-temporary, we would record a charge to the consolidated statement of operations as appropriate.

Our financial assets and liabilities measured at fair value on a recurring basis are as follows:

Ìý

Ìý ÌýÌý Fair value measurements as of MarchÌý31, 2012 Ìý
(in thousands) ÌýÌý QuotedÌýprices
in active
markets for
identical
assets

(LevelÌý1)
Ìý ÌýÌý Significant
other
observable
inputs

(LevelÌý2)
Ìý ÌýÌý Significant
unobservable
inputs

(LevelÌý 3)
Ìý ÌýÌý Total Ìý

Assets:

ÌýÌý ÌýÌý ÌýÌý ÌýÌý

Money market funds

ÌýÌý $ 22,450 ÌýÌý ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ 22,450 ÌýÌý

US Treasury securities

ÌýÌý Ìý 24,997 ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 24,997 ÌýÌý

BNZE Note and beneficial conversion feature

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 1,700 ÌýÌý ÌýÌý Ìý 1,700 ÌýÌý

BNZE common stock warrants

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 1,063 ÌýÌý ÌýÌý Ìý 1,063 ÌýÌý

Neovasc common stock options

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 1,139 ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 1,139 ÌýÌý

Neovasc common stock warrants

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 868 ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 868 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Total assets

ÌýÌý $ 47,447 ÌýÌý ÌýÌý $ 2,007 ÌýÌý ÌýÌý $ 2,763 ÌýÌý ÌýÌý $ 52,217 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Liabilities:

ÌýÌý ÌýÌý ÌýÌý ÌýÌý

Forward contracts

ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ 87 ÌýÌý ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ 87 ÌýÌý

URNA contingent consideration

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 510 ÌýÌý ÌýÌý Ìý 510 ÌýÌý

Claros contingent consideration

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 13,721 ÌýÌý ÌýÌý Ìý 13,721 ÌýÌý

FineTech contingent consideration

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 4,915 ÌýÌý ÌýÌý Ìý 4,915 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Total Liabilities

ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ 87 ÌýÌý ÌýÌý $ 19,146 ÌýÌý ÌýÌý $ 19,233 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

The following table reconciles the beginning and ending balances of our Level 3 assets and liabilities:

Ìý

(in thousands) ÌýÌý BNZE
Note and
BZNE
Warrants
Ìý ÌýÌý Contingent
consideration
Ìý

Beginning balance

ÌýÌý $ —ÌýÌý ÌýÌý ÌýÌý $ 18,002 ÌýÌý

Additions

ÌýÌý Ìý 1,700 ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý

Change in fair value included in:

ÌýÌý ÌýÌý

Statement of operations

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý 1,144 ÌýÌý

Other income and expense, net

ÌýÌý Ìý 1,063 ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Ending balance

ÌýÌý $ 2,763 ÌýÌý ÌýÌý $ 19,146 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Ìý

18


Table of Contents

NOTE 8 DERIVATIVE CONTRACTS

We enter into foreign currency forward exchange contracts to cover the risk of exposure to exchange rate differences arising from inventory purchases on letters of credit. Under these forward contracts, for any rate above or below the fixed rate, we receive or pay the difference between the spot rate and the fixed rate for the given amount at the settlement date.

In January 2012, we entered into a foreign exchange, fixed interest rate swap contract that provides for us to pay a fixed interest rate on the underlying loan balance denominated in Chilean Pesos. We entered into this agreement in Chile for purchases of inventory denominated in U.S. dollars. A hypothetical 1% interest rate change or 10% foreign exchange rate change will not have a material impact on our results from operations or financial position.

We record derivative financial instruments on our balance sheet at their fair value and the effect on loss is recorded in other accrued expenses and the changes in the fair value are recognized in other income expense, net. To qualify the derivative instrument as a hedge, we are required to meet strict hedge effectiveness and contemporaneous documentation requirements at the initiation of the hedge and assess the hedge effectiveness on an ongoing basis over the life of the hedge. At MarchÌý31, 2012, the forward contracts did not meet the documentation requirements to be designated as hedges. Accordingly, we recognize all changes in fair values in income.

The Neovasc warrants are accounted for as derivatives as they are readily convertible into cash. As a result, the fluctuations in fair value are recorded in our statement of operations in other income and expense as an unrealized gain or loss. During the three months ended MarchÌý31, 2012, we recorded an unrealized gain of approximately $0.1 million in other income and expense to reflect the change in fair value based on the increase in NeovascÂ’s stock price. We value the warrants based on the Black-Scholes-Merton valuation model. In addition, the conversion feature of the BZNE Note and BZNE Warrants also are accounted for as derivatives and the changes in their fair value will be recorded in our statement of operations in other income and expense. We did not record any change in fair value of either the conversion feature of the BZNE Note or BZNE Warrants during the three months ended MarchÌý31, 2012.

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The outstanding contracts at MarchÌý31, 2012, have been recorded at fair value, and their maturity details are as follows:

Ìý

(in thousands)

Days until maturity

ÌýÌý ContractÌývalue Ìý ÌýÌý FairÌývalueÌýat
MarchÌý31,Ìý 2012
Ìý ÌýÌý EffectÌýonÌýloss Ìý

0 to 30

ÌýÌý $ 911 ÌýÌý ÌýÌý $ 948 ÌýÌý ÌýÌý $ (37 )Ìý

31 to 60

ÌýÌý Ìý 1,368 ÌýÌý ÌýÌý Ìý 1,395 ÌýÌý ÌýÌý Ìý (27 )Ìý

61 to 90

ÌýÌý Ìý 515 ÌýÌý ÌýÌý Ìý 536 ÌýÌý ÌýÌý Ìý (21 )Ìý

91 to 120

ÌýÌý Ìý 138 ÌýÌý ÌýÌý Ìý 140 ÌýÌý ÌýÌý Ìý (2 )Ìý

121 to 180

ÌýÌý Ìý 249 ÌýÌý ÌýÌý Ìý 249 ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý

More than 180

ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý ÌýÌý Ìý —ÌýÌý ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

Total

ÌýÌý $ 3,181 ÌýÌý ÌýÌý $ 3,268 ÌýÌý ÌýÌý $ (87 )Ìý
ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý ÌýÌý

Ìý

Ìý

Ìý

NOTE 9 RELATED PARTY TRANSACTIONS

In February 2012, we made a $1.0 million investment in ChromaDex. Other investors participating in the private financing included the Gamma Trust, Hsu Gamma, and Richard Lerner, a director. Curt Lockshin, СÖíÊÓƵappÂ’s Vice President, Corporate R&D Initiatives, serves as a director for ChromaDex. Following our investment, we own 1.5% of ChromaDex, the Gamma Trust owns approximately 16% of ChromaDex; Hsu Gamma owns approximately 1%; and each of Dr.ÌýLerner, Richard Pfenniger, Jr., Steven Rubin, and Rao Uppaluri own less than 1% of ChromaDex. Refer to Note 5.

In February 2012, we purchased from BZNE $1.7 million of 10% secured convertible promissory notes (the “Notes”), convertible into BZNE common stock at a price equal to $0.20 per common share, which Notes are due and payable on FebruaryÌý24, 2014 and ten year warrants to purchase 8.5Ìýmillion shares of BZNE common stock at an exercise price of $0.40 per share. Refer to Note 5.

Roberto Prego Novo is the Chairman of BZNE and presently serves as a Consultant to СÖíÊÓƵapp. Dr.ÌýFrost and Mr.ÌýPrego Novo previously invested in BZNE in February and March, 2011. On MayÌý16, 2011, BZNE acquired the assets and assumed the liabilities of Aero Pharmaceuticals, Inc. (“Aero”) in exchange for which BZNE issued an aggregate of 8,331,396 shares of its restricted common stock to Aero. On SeptemberÌý21, 2011, BZNE issued an additional 13,914 shares to Aero due to the late filing of a registration statement. Prior to the transaction, Dr.ÌýFrost, through the Gamma Trust, beneficially owned approximately 46% of AeroÂ’s issued and outstanding capital stock; Mr.ÌýPrego Novo owned approximately 23% of AeroÂ’s issued and outstanding capital stock through Olyrca Trust; and Dr.ÌýHsiao beneficially owned approximately 12% of AeroÂ’s issued and outstanding stock. Each of Drs. Frost and Hsiao and Mr.ÌýPrego Novo beneficially owned approximately 9.2%, 1.7%, and 8.2% of BZNE, respectively, following the purchase of Aero by BZNE. Each of Dr.ÌýUppaluri and Mr.ÌýRubin beneficially own less than 1% of BZNE as a result of their prior ownership of Aero shares. Effective AprilÌý18, 2012, Dr.ÌýFrost, through the Gamma Trust, also made a loan to BZNE in the principal amount of $250,000, with a maturity date of AugustÌý7, 2012, which is secured by a first priority lien on a particular BZNE receivable.

On AugustÌý17, 2011, we made an investment in Neovasc. Refer to Note 5. Dr.ÌýFrost and other members of СÖíÊÓƵapp management are shareholders of Neovasc. Prior to the investment, Dr.ÌýFrost beneficially owned approximately 36% of Neovasc, Dr.ÌýJane Hsiao owned approximately 6%, and each of Dr.ÌýUppaluri and Mr.ÌýRubin owned less than 1%. Dr.ÌýJane Hsiao and Steven Rubin also serve on the board of directors for Neovasc.

On MarchÌý14, 2011, we issued 27,000,000 shares of our common stock. Refer to Note 7. The 27,000,000 shares of our common stock issued include an aggregate of 3,733,000 shares of our common stock purchased by the Gamma Trust and Hsu Gamma at the public offering price. The Gamma Trust purchased an aggregate of 3,200,000 shares for approximately $12.0 million, and Hsu Gamma purchased an aggregate of 533,000 shares for approximately $1.9 million. JefferiesÌý& Company, Inc. and J.P. Morgan Securities LLC acted as joint book-running managers for the offering. UBS Investment Bank and Lazard Capital Markets LLC acted as co-lead managers for the offering and Ladenburg ThalmannÌý& Co. Inc., a subsidiary of Ladenburg Thalmann Financial Services Inc., acted as co-manager for the offering. Dr.ÌýFrost is the Chairman of the Board of Directors and principal shareholder of Ladenburg Thalmann Financial Services Inc.

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In January 2011, we entered into a definitive agreement with CURNA and each of CURNAÂ’s stockholders and option holders, pursuant to which we agreed to acquire all of the outstanding stock of CURNA in exchange for $10.0 million in cash, plus $0.6 million in liabilities, of which $0.5 million was paid at closing. At the time of the transaction, The Scripps Research Institute (“TSRI”) owned approximately 4% of CURNA. Dr.ÌýFrost serves as a Trustee for TSRI and Dr.ÌýRichard Lerner, a director of the Company, served as its President until DecemberÌý2011.

Our unutilized $12.0 million line of credit with the Frost Group, LLC (the “Frost Group”) expired on MarchÌý31, 2012. The Frost Group members include a trust controlled by Dr.ÌýFrost, who is the CompanyÂ’s Chief Executive Officer and Chairman of the board of directors, Dr.ÌýJaneÌýH. Hsiao, who is the Vice Chairman of the board of directors and Chief Technical Officer, Steven D. Rubin who is Executive Vice President — Administration and a director of the Company, and Rao Uppaluri, who is the Chief Financial Officer of the Company. On JuneÌý2, 2010 we repaid all amounts outstanding on the line of credit including $12.0 million in principal and $4.1 million in interest. We did not have any borrowings under the line of credit at any time during the 2011 or 2012 fiscal years. We were obligated to pay interest upon maturity, capitalized quarterly, on any outstanding borrowings under the line of credit at an 11% annual rate. The line of credit was collateralized by all of our U.S. personal property except our intellectual property.

In NovemberÌý2010, we made an investment in Fabrus, Inc., a privately held early stage biotechnology company with next generation therapeutic antibody drug discovery and development capabilities. In exchange for the investment, we acquired approximately 13% of Fabrus on a fully diluted basis. Our investment was part of a $2.1 million financing for Fabrus. Other investors participating in the financing include the Gamma Trust and Hsu Gamma. In connection with the financing, Drs. Frost and Hsiao joined the Fabrus Board of Managers. Dr.ÌýRichard Lerner, a director of the Company, owns approximately 5% of Fabrus. Vaughn Smider, Founder and CEO of Fabrus, is an Assistant Professor at The Scripps Research Institute (“TSRI”). Dr.ÌýFrost serves as a Trustee for TSRI and Dr. Richard Lerner served as its President until DecemberÌý2011.

On JulyÌý20, 2010, we entered into a use agreement for approximately 1,100 square feet of space in Jupiter, Florida to house our molecular diagnostics operations with TSRI. Dr.ÌýFrost is a member of the Board of Trustees of TSRI and Dr.ÌýRichard Lerner, a member of our Board of Directors, was the President of TSRI until DecemberÌý2011. Pursuant to the terms of the use agreement, which was effective as of NovemberÌý1, 2009, gross rent was approximately $40 thousand per year for a two-year term. We ceased use of this space in SeptemberÌý2011.

On JuneÌý1, 2010, we entered into a cooperative research and development agreement with Academia Sinica in Taipei, Taiwan (“Academia Sinica”), for pre-clinical work for a compound against various forms of cancer. Dr.ÌýAlice Yu, a member of our Board of Directors, is a Distinguished Research Fellow and Associate Director at the Genomics Research Center, Academia Sinica (“Genomics Research Center”). In connection with the agreement, we are required to pay Academia Sinica approximately $0.2 million over the term of the agreement.

On JulyÌý20, 2009, we entered into a worldwide exclusive license agreement with Academia Sinica for a new technology to develop protein vaccines against influenza and other viral infections. Dr.ÌýAlice Yu, a member of our Board of Directors, is a Distinguished Research Fellow and Associate Director at the Genomics Research Center. Effective MarchÌý5, 2010, the Frost Group assigned two license agreements with Academia Sinica to us. The license agreements pertain to alpha-galactosyl ceramide analogs and their use as immunotherapies and peptide ligands in the diagnosis and treatment of cancer. In connection with the assignment of the two licenses, we agreed to reimburse the Frost Group for the licensing fees previously paid by the Frost Group to Academia Sinica in the amounts of $50 thousand and $75 thousand, respectively, as well as reimbursement of certain expenses of $50 thousand.

Effective SeptemberÌý21, 2009, we entered into an agreement pursuant to which we invested $2.5 million in Cocrystal in exchange for 1,701,723 shares of CocrystalÂ’s Convertible Series A Preferred Stock. A group of investors, led by the Frost Group (the “Cocrystal Investors”), previously invested $5 million in Cocrystal, and agreed to invest an additional $5 million payable in two equal installments in SeptemberÌý2009 and MarchÌý2010. As a result of an amendment to the Cocrystal Investors agreements dated JuneÌý9, 2009, the Company, rather than the Cocrystal Investors, made the first installment investment ($2.5 million) on SeptemberÌý21, 2009. Refer to Note 5.

On JuneÌý16, 2009, we entered into an agreement to lease approximately 10,000 square feet of space in Hialeah, Florida to house manufacturing and service operations for our ophthalmic instrumentation business (the “Hialeah Facility”) from an entity controlled by Drs. Frost and Hsiao. Effective as of JulyÌý1, 2011, the lease was amended to include an additional 5,000 square feet of space at the same rate per square foot as was then in effect under the lease. Following the amendment, gross rent payable under the lease was $0.2 million per year. Upon the closing of the sale of our instrumentation business to Optos, we assigned the lease to Optos. Refer to NoteÌý6.

Ìý

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On JuneÌý10, 2009, we entered into a stock purchase agreement with Sorrento, pursuant to which we invested $2.3 million in Sorrento. Refer to Note 5. In exchange for the investment, we acquired approximately one-third of the outstanding common shares of Sorrento and received a fully-paid, exclusive license to the Sorrento antibody library for the discovery and development of therapeutic antibodies in the field of ophthalmology. On SeptemberÌý21, 2009, Sorrento entered into a merger transaction with Quikbyte Software, Inc. Prior to the merger transaction, certain investors, including Dr.ÌýFrost and other members of СÖíÊÓƵapp management, made an investment in Quikbyte. Dr.ÌýRichard Lerner, a member of our Board of Directors, serves as a consultant and scientific advisory board member to Sorrento and owns less than one percent of its shares.

In NovemberÌý2007, we entered into an office lease with Frost Real Estate Holdings, LLC, an entity affiliated with Dr.ÌýFrost. The lease is for approximately 8,300 square feet of space in an office building in Miami, Florida, where the CompanyÂ’s principal executive offices are located. We had previously been leasing this space from Frost Real Estate Holdings on a month-to-month basis while the parties were negotiating the lease. The lease provides for payments of approximately $18 thousand per month in the first year increasing annually to $24 thousand per month in the fifth year, plus applicable sales tax. The rent is inclusive of operating expenses, property taxes and parking. The rent for the first year was reduced to reflect a $30 thousand credit for the costs of tenant improvements.

We reimburse Dr.ÌýFrost for Company-related use by Dr.ÌýFrost and our other executives of an airplane owned by a company that is beneficially owned by Dr.ÌýFrost. We reimburse Dr.ÌýFrost in an amount equal to the cost of a first class airline ticket between the travel cities for each executive, including Dr.ÌýFrost, traveling on the airplane for Company-related business. We do not reimburse Dr.ÌýFrost for personal use of the airplane by Dr.ÌýFrost or any other executive; nor do we pay for any other fixed or variable operating costs of the airplane. We reimbursed Dr.ÌýFrost approximately $65 thousand and $57 thousand, respectively, for Company-related travel by Dr.ÌýFrost and other СÖíÊÓƵapp executives during the three months ended MarchÌý31, 2012 and 2011.

NOTE 10 COMMITMENTS AND CONTINGENCIES

In connection with our acquisitions of CURNA, Claros and FineTech, we agreed to pay future consideration to the sellers upon the achievement of certain events. As a result, we recorded $19.1 million as contingent consideration with $4.3Ìýmillion recorded within accrued expenses and $14.8 million recorded within other long-term liabilities. Refer to Note 5.

In connection with the acquisition of Vidus Ocular, Inc. (“Vidus”), we agreed to issue additional stock consideration upon the occurrence of certain events including the issuance of 488,420 shares of our common stock upon the achievement of certain development milestones and, in the event that the stock price for our common stock at the time of receipt of approval or clearance by the FDA of a pre-market notification 510(k) relating to the Aquashunt™ is not at or above a specified price, we will be obligated to issue an additional 413,850 shares of our common stock.

We are a party to litigation in the ordinary course of business. We do not believe that any such litigation will have a material adverse effect on our business, financial condition, or results of operations.

We expect to incur substantial losses as we continue the development of our product candidates, continue our other research and development activities, and establish a sales and marketing infrastructure in anticipation of the commercialization of our diagnostic and pharmaceutical product candidates. We currently have limited commercialization capabilities, and it is possible that we may never successfully commercialize any of our diagnostic and pharmaceutical product candidates. We do not currently generate revenue from any of our diagnostic and pharmaceutical product candidates. Our research and development activities are budgeted to expand over a period of time and will require further resources if we are to be successful. As a result, we believe that our operating losses are likely to be substantial over the next several years. We may need to obtain additional funds to further develop our research and development programs, and there can be no assurance that additional capital will be available to us on acceptable terms, or at all.

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NOTE 11 SEGMENTS

We currently manage our operations in one reportable segment, pharmaceutical. The pharmaceutical segment consists of two operating segments, our (i)Ìýpharmaceutical research and development segment which is focused on the research and development of pharmaceutical products, diagnostic tests and vaccines, and (ii)Ìýthe pharmaceutical operations we acquired in Chile, Mexico, and Israel through the acquisition of СÖíÊÓƵapp Chile, Exakta-СÖíÊÓƵapp, and FineTech, respectively. There are no inter-segment sales. We evaluate the performance of each segment based on operating profit or loss. There is no inter-segment allocation of interest expense and income taxes. We previously recorded our ophthalmic instrumentation business as its own reporting segment.

Information regarding our operations and assets for the two segments and the unallocated corporate operations as well as geographic information are as follows:

Ìý

Ìý ÌýÌý For the three months ended
MarchÌý31,
Ìý
(in thousands) ÌýÌý 2012 Ìý Ìý 2011 Ìý

Operating (loss) income from continuing operations

ÌýÌý Ìý

Pharmaceutical

ÌýÌý $ (6,031 )Ìý Ìý $ (1,019 )Ìý

Corporate

ÌýÌý Ìý (2,816 )Ìý Ìý Ìý (3,117 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý
ÌýÌý $ (8,847 )Ìý Ìý $ (4,136 )Ìý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Depreciation and amortization

ÌýÌý Ìý

Pharmaceutical

ÌýÌý $ 2,284 ÌýÌý Ìý $ 826 ÌýÌý

Corporate

ÌýÌý Ìý 44 ÌýÌý Ìý Ìý 43 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý
ÌýÌý $ 2,328 ÌýÌý Ìý $ 869 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

Product sales

ÌýÌý Ìý

United States

ÌýÌý $ —ÌýÌý ÌýÌý Ìý $ —ÌýÌý ÌýÌý

Chile

ÌýÌý Ìý 5,701 ÌýÌý Ìý Ìý 5,751 ÌýÌý

Israel

ÌýÌý Ìý 1,627 ÌýÌý Ìý Ìý —ÌýÌý ÌýÌý

Mexico

ÌýÌý Ìý 1,311 ÌýÌý Ìý Ìý 1,199 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý
ÌýÌý $ 8,639 ÌýÌý Ìý $ 6,950 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý
Ìý ÌýÌý As of Ìý
Ìý ÌýÌý MarchÌý31,
2012
Ìý Ìý DecemberÌý31,
2011
Ìý

Assets

ÌýÌý Ìý

Pharmaceutical

ÌýÌý $ 165,667 ÌýÌý Ìý $ 154,437 ÌýÌý

Corporate

ÌýÌý Ìý 65,903 ÌýÌý Ìý Ìý 75,048 ÌýÌý

Discontinued operations

ÌýÌý Ìý —ÌýÌý ÌýÌý Ìý Ìý 4 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý
ÌýÌý $ 231,570 ÌýÌý Ìý $ 229,489 ÌýÌý
ÌýÌý

Ìý

Ìý

Ìý Ìý

Ìý

Ìý

Ìý

During the three months ended MarchÌý31, 2012, no customer represented more than 10% of our total revenue. During the three months ended MarchÌý31, 2011, our largest customer represented 12% of our total revenue. As of MarchÌý31, 2012, one customer represented 23% of our accounts receivable balance. As of DecemberÌý31, 2011, one customer represented 29% of our accounts receivable balance.

NOTE 12 SUBSEQUENT EVENTS

In AprilÌý2012, we completed the acquisition of ALS Distribuidora Limitada (“ALS”), a privately-held Chilean pharmaceutical company, pursuant to a stock purchase agreement entered into in JanuaryÌý2012. In connection with the transaction, we agreed to pay up to a total of $4.0 million in cash to the Sellers. Pursuant to the purchase agreement, we paid (i)Ìý$2.4 million in cash at closing to the Sellers, less certain liabilities, and (ii)Ìý$0.8 million in cash at closing into a separate escrow account to satisfy possible indemnity claims. We agreed to pay an additional $0.8 million, the remainder of the $4.0 million purchase price, to the Sellers upon the legal registration in the name of ALS of certain trademarks and product registrations previously held by Arama Laboratorios y Compañía Limitada.

Ìý

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We have reviewed all subsequent events and transactions that occurred after the date of our MarchÌý31, 2012 consolidated balance sheet date, through the time of filing this Quarterly Report on Form 10-Q.

ItemÌý2. ManagementÂ’s Discussion and Analysis of Financial Condition and Results of Operations

OVERVIEW

You should read this discussion together with the condensed consolidated financial statements, related Notes, and other financial information included elsewhere in this report and in our Annual Report on Form 10-K for the year ended DecemberÌý31, 2011 (the “Form 10-K”). The following discussion contains assumptions, estimates and other forward-looking statements that involve a number of risks and uncertainties, including those discussed under “Risk Factors,” in Part II, ItemÌý1A of our Form 10-K for the year ended DecemberÌý31, 2011. These risks could cause our actual results to differ materially from those anticipated in these forward-looking statements.

We are a multi-national pharmaceutical and diagnostics company that seeks to establish industry-leading positions in large and rapidly growing medical markets by leveraging our discovery, development and commercialization expertise and our novel and proprietary technologies. We are developing a range of solutions to diagnose, treat and prevent various conditions, including molecular diagnostics tests, point-of-care tests, and proprietary pharmaceuticals and vaccines. We plan to commercialize these solutions on a global basis in large and high growth markets, including emerging markets. We have already established emerging markets pharmaceutical platforms in Chile and Mexico, which are generating revenue and which we expect to generate positive cash flow and facilitate future market entry for our products currently in development. We also operate a specialty active pharmaceutical ingredients (“APIs”) manufacturer in Israel, which is currently generating revenue and positive cash flow, and which we expect will play a valuable role in the development of our pipeline of peptoids and other molecules for our proprietary molecular diagnostic and therapeutic products. We continue to actively explore opportunities to acquire complementary pharmaceuticals, compounds, technologies, and businesses.

We expect to incur substantial losses as we continue the development of our product candidates, continue our other research and development activities, and establish a sales and marketing infrastructure in anticipation of the commercialization of our diagnostic and pharmaceutical product candidates. We currently have limited commercialization capabilities, and it is possible that we may never successfully commercialize any of our diagnostic and pharmaceutical product candidates. We do not currently generate revenue from any of our diagnostic and pharmaceutical product candidates. Our research and development activities are budgeted to expand over a period of time and will require further resources if we are to be successful. As a result, we believe that our operating losses are likely to be substantial over the next several years. We may need to obtain additional funds to further develop our research and development programs, and there can be no assurance that additional capital will be available to us when needed on acceptable terms, or at all.

RECENT DEVELOPMENTS

In AprilÌý2012, we completed the acquisition of ALS Distribuidora Limitada (“ALS”), a privately-held Chilean pharmaceutical company, pursuant to a stock purchase agreement entered into in JanuaryÌý2012. In connection with the transaction, we agreed to pay up to a total of $4.0 million in cash to the Sellers. Pursuant to the purchase agreement, we paid (i)Ìý$2.4 million in cash at closing to the Sellers, less certain liabilities, and (ii)Ìý$0.8 million in cash at closing into a separate escrow account to satisfy possible indemnity claims. We agreed to pay an additional $0.8 million, the remainder of the $4.0 million purchase price, to the Sellers upon the legal registration in the name of ALS of certain trademarks and product registrations previously held by Arama Laboratorios y Compañía Limitada (“Arama”).

Recently, we announced a collaboration with Laboratory Corporation of America (LabCorp®), a S&P 500 company and pioneer in commercializing new diagnostic technologies, for Labcorp to complete the development and later commercialize laboratory testing services for Alzheimer’s disease. We will continue to develop (on our own or with partners) in vitro diagnostic tests for detection of Alzheimer’s disease, as well as companion diagnostic applications for the Alzheimer’s test, all of which rights were retained by us under the Labcorp agreement.

Ìý

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RESULTS OF OPERATIONS

FOR THE THREE MONTHS ENDED MARCHÌý31, 2012 AND 2011

Revenue. Revenue for the three months ended MarchÌý31, 2012, was $8.8 million, compared to $7.0 million for the comparable 2011 period. The increase in revenue during the first three months of 2012 is primarily due to revenue generated by our Israeli Active Pharmaceutical Ingredient (“API”) manufacturer which we acquired in December 2011.

Gross margin. Gross margin for the three months ended MarchÌý31, 2012, was $3.8 million compared to $2.8 million for the comparable period of 2011. Gross margin for the three months ended MarchÌý31, 2012, increased from the 2011 period primarily as a result of the increased gross margin generated by our pharmaceutical businesses in Israel and Mexico, partially offset by decreased gross margin generated by our pharmaceutical business in Chile principally due to increased inventory reserves. Gross Margin for the three months ended March 31, 2012 benefited from the correction of an error related to certain costs for inventory purchases. The correction of the error resulted in an increase of gross margin of $0.4 million, or $0.00 per share.

Selling, general and administrative expense. Selling, general and administrative expense for the three months ended MarchÌý31, 2012, was $4.7 million compared to $5.1 million of expense for the comparable period of 2011. The decrease in selling, general and administrative expenses is primarily the result of decreased equity-based compensation expense partially offset by increased professional fees and activities related to our Israeli API business. Selling, general and administrative expenses during the first three months of 2012 and 2011 primarily consist of personnel expenses and professional fees, including equity-based compensation expense of $0.6 million and $1.4 million, respectively, and professional fees.

Research and development expense. Research and development expense during the three months ended MarchÌý31, 2012 and 2011, was $4.8 million and $1.1 million, respectively. The increase in research and development expense primarily reflects increased activities related to our Claros, CURNA and molecular diagnostics research and development programs. We acquired Claros in October 2011, and we have also increased staffing and related activities for our CURNA and molecular diagnostics development programs. The three months ended MarchÌý31, 2012 and 2011, include equity-based compensation expense of $0.6 million and $0.4 million, respectively. Research and development expense for the three months ended MarchÌý31, 2011 primarily consisted of activities related to our molecular diagnostics development programs and post-acquisition activities related to CURNA.

Contingent consideration expense. Contingent consideration expense for the three months ended MarchÌý31, 2012 was $1.1 million, which represents the change in the fair value of the contingent consideration liability due to the time value of money. The contingent consideration liability relates to potential amounts payable to Claros and FineTechÂ’s former stockholders pursuant to our agreement to acquire them in October and December 2011, respectively. The comparable period of 2011 did not include any such expense.

Other operating expenses. Other operating expense was $2.0 million for the three months ended MarchÌý31, 2012 compared to $0.8 million for the comparable period ended MarchÌý31, 2011. Other operating expenses primarily include the amortization of intangible assets. Amortization expense increased due to the October and December 2011 acquisitions of Claros and FineTech, respectively.

Other income and expenses. Other income and expense, net was $1.0 million for the first three months of 2012 compared to other income, net of $43 thousand for the comparable 2011 period. The first three months of 2012 include $1.1 million of other income recognized from the fair value of the warrants received in connection with our investment in Biozone Pharmaceuticals, Inc. Other income primarily consists of interest earned on our cash and cash equivalents and other expense primarily reflects the interest incurred on our lines of credit in Chile. Partially offsetting the interest incurred on our Chilean lines of credit was the benefit of our Chilean and Mexican operations currencies during the three months ended MarchÌý31, 2012.

Discontinued operations. Loss from discontinued operations was $0 compared to $1.0 million for the three months ended MarchÌý31, 2012 and the comparable period of 2011, respectively. The 2011 results reflect the operating loss of our instrumentation business for that period. In October 2011 we sold the instrumentation business and no longer have any ongoing operations related to that business.

Income taxes. Our income tax provision reflects the income tax payable in Chile and Mexico. Our Israeli operations will benefit from a tax holiday during 2012. We have recorded a full valuation allowance against our deferred tax assets in the U.S.

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LIQUIDITY AND CAPITAL RESOURCES

At MarchÌý31, 2012, we had cash, cash equivalents and marketable securities of approximately $62.1Ìýmillion. Cash used in operations during 2012 primarily reflects expenses related to selling, general and administrative activities related to our corporate operations and research and development activities, as well as our operations in Chile, Israel and Mexico. In addition, we invested $2.7 million in two pharmaceutical businesses. Since our inception, we have not generated sufficient gross margins to offset our operating and other expenses and our primary source of cash has been from the public and private placement of stock and credit facilities available to us.

In connection with our acquisitions of CURNA, Claros and FineTech, we agreed to pay future consideration to the sellers upon the achievement of certain events, including minimum cash payments of $5.0 to the former stockholder of FineTech upon the achievement of certain sales milestones, and up to an additional $19.1 million in shares of the our common stock to the former stockholders of Claros upon and subject to the achievement of certain milestones.

As of MarchÌý31, 2012, we have outstanding lines of credit in the aggregate amount of $14.2Ìýmillion with 7 financial institutions in Chile, with an additional $5.2 million available for additional borrowings. The average interest rate on these lines of credit is approximately 7%. These lines of credit are short-term and are generally due within three months. These lines of credit are used primarily as a source of working capital for inventory purchases. The highest balance at any time during the three months ended MarchÌý31, 2012 was $14.7Ìýmillion. We intend to continue to enter into these lines of credit as needed. There is no assurance that these lines of credit or other funding sources will be available to us on acceptable terms, or at all, in the future.

Our unutilized $12.0Ìýmillion line of credit with the Frost Group expired on MarchÌý31, 2012. We were obligated to pay interest upon maturity, capitalized quarterly, on any outstanding borrowings under the line of credit at an 11% annual rate. The line of credit was collateralized by all of our U.S. based personal property except our intellectual property and had no amounts borrowed after JuneÌý2, 2010 when it was repaid in full.

We expect to incur losses from operations for the foreseeable future. We expect to incur substantial research and development expenses, including expenses related to the hiring of personnel and additional clinical trials. We expect that selling, general and administrative expenses will also increase as we expand our sales, marketing and administrative staff and add infrastructure.

We believe the cash, cash equivalents, and marketable securities on hand at MarchÌý31, 2012 and the amounts available to be borrowed under our lines of credit are sufficient to meet our anticipated cash requirements for operations and debt service beyond the next 12Ìýmonths. We based this estimate on assumptions that may prove to be wrong or are subject to change, and we may be required to use our available cash resources sooner than we currently expect. If we acquire additional assets or companies, accelerate our product development programs or initiate additional clinical trials, we will need additional funds. Our future cash requirements will depend on a number of factors, including possible acquisitions, the continued progress of research and development of our product candidates, the timing and outcome of clinical trials and regulatory approvals, the costs involved in preparing, filing, prosecuting, maintaining, defending, and enforcing patent claims and other intellectual property rights, the status of competitive products, the availability of financing, and our success in developing markets for our product candidates. If we are not able to secure additional funding when needed, we may have to delay, reduce the scope of, or eliminate one or more of our clinical trials or research and development programs or possible acquisitions.

We intend to finance additional research and development projects, clinical trials and our future operations with a combination of available cash on hand, payments from potential strategic research and development, licensing and/or marketing arrangements, public offerings, private placements, debt financing and revenues from future product sales, if any. There can be no assurance, however, that additional capital will be available to us on acceptable terms, or at all.

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CRITICAL ACCOUNTING POLICIES AND ESTIMATES

Accounting estimates. The preparation of financial statements in conformity with generally accepted accounting principles requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of sales and expenses during the reporting period. Actual results could differ from those estimates.

Equity-based compensation. We recognize equity based compensation as an expense in our financial statements and that cost is measured at the fair value of the awards and expensed over their vesting period. Equity-based compensation arrangements to non-employees are recorded at their fair value on the measurement date. We estimate the grant-date fair value of our stock option grants using a valuation model known as the Black-Scholes-Merton formula or the “Black-Scholes Model” and allocate the resulting compensation expense over the corresponding requisite service period associated with each grant. The Black-Scholes Model requires the use of several variables to estimate the grant-date fair value of stock options including expected term, expected volatility, expected dividends and risk-free interest rate. We perform significant analyses to calculate and select the appropriate variable assumptions used in the Black-Scholes Model. We also perform significant analyses to estimate forfeitures of equity-based awards. We are required to adjust our forfeiture estimates on at least an annual basis based on the number of share-based awards that ultimately vest. The selection of assumptions and estimated forfeiture rates is subject to significant judgment and future changes to our assumptions and estimates may have a material impact on our Consolidated Financial Statements.

Goodwill and intangible assets. The allocation of the purchase price for acquisitions requires extensive use of accounting estimates and judgments to allocate the purchase price to the identifiable tangible and intangible assets acquired, including in-process research and development, and liabilities assumed based on their respective fair values. Additionally, we must determine whether an acquired entity is considered to be a business or a set of net assets, because a portion of the purchase price can only be allocated to goodwill in a business combination.

Appraisals inherently require significant estimates and assumptions, including but not limited to, determining the timing and estimated costs to complete the in-process research and development projects, projecting regulatory approvals, estimating future cash flows, and developing appropriate discount rates. We believe the estimated fair values assigned to the Claros and FineTech assets acquired and liabilities assumed are based on reasonable assumptions. However, the fair value estimates for the purchase price allocation may change during the allowable allocation period, which is up to one year from the acquisition date, if additional information becomes available that would require changes to our estimates.

Allowance for doubtful accounts and revenue recognition. Generally, we recognize revenue from product sales when goods are shipped and title and risk of loss transfer to our customers. Our estimates for sales returns are based upon the historical patterns of products returned matched against the sales from which they originated, and managementÂ’s evaluation of specific factors that may increase the risk of product returns. We analyze accounts receivable and historical bad debt levels, customer credit worthiness and current economic trends when evaluating the adequacy of the allowance for doubtful accounts using the specific identification method. Our reported net loss is directly affected by managementÂ’s estimate of the collectability of accounts receivable. The allowance for doubtful accounts recognized in our consolidated balance sheets at MarchÌý31, 2012 and DecemberÌý31, 2011 was $0.3 million and $0.4 million, respectively.

Recent accounting pronouncements. On JanuaryÌý1, 2012, we adopted an amendment issued by the Financial Accounting Standards Board (“FASB”) to the accounting standards related to fair value measurements and disclosure requirements. This standard provides certain amendments to the existing guidance on the use and application of fair value measurements and maintains a definition of fair value that is based on the notion of exit price. The adoption of this standard did not have a material impact on our consolidated financial statements.

On JanuaryÌý1, 2012, we adopted amendments issued by the FASB to the accounting standards related to the presentation of comprehensive income. These standards revise the manner in which entities present comprehensive income in their financial statements and remove the option to present items of other comprehensive income in the statement of changes in stockholdersÂ’ equity. These standards require an entity to report components of comprehensive income in either (1)Ìýa continuous statement of comprehensive income, or (2)Ìýtwo separate but consecutive statements of net income and other comprehensive income. We modified our financial statements presentation using the latter alternative.

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On JanuaryÌý1, 2012, we adopted revised guidance issued by the FASB related to the testing of goodwill for impairment. Under the revised guidance, an entity has the option to perform a qualitative assessment of whether it is more-likely-than-not that a reporting unitÂ’s fair value is less than its carrying value prior to performing the two-step quantitative goodwill impairment test. If, based on the qualitative factors, an entity determines that the fair value of the reporting unit is greater than its carrying amount, then the entity would not be required to perform the two-step quantitative impairment test for that reporting unit. However, if the qualitative assessment indicates that it is not more-likely-than-not that the reporting unitÂ’s fair value exceeds its carrying value, then the quantitative assessment must be performed. An entity is permitted to perform the qualitative assessment on none, some or all of its reporting units and may also elect to bypass the qualitative assessment and begin with the quantitative assessment of goodwill impairment. This amendment did not have a material impact on our consolidated financial statements.

ItemÌý3. Quantitative and Qualitative Disclosures About Market Risk

In the normal course of doing business, we are exposed to the risks associated with foreign currency exchange rates and changes in interest rates.

Foreign Currency Exchange Rate Risk – Although we do not speculate in the foreign exchange market, we may from time to time manage exposures that arise in the normal course of business related to fluctuations in foreign currency exchange rates by entering into offsetting positions through the use of foreign exchange forward contracts. Certain firmly committed transactions are hedged with foreign exchange forward contracts. As exchange rates change, gains and losses on the exposed transactions are partially offset by gains and losses related to the hedging contracts. Both the exposed transactions and the hedging contracts are translated at current spot rates, with gains and losses included in earnings.

Our derivative activities, which consist of foreign exchange forward contracts and swaps, are initiated to hedge forecasted cash flows that are exposed to foreign currency risk. The foreign exchange forward contracts generally require us to exchange local currencies for foreign currencies based on pre-established exchange rates at the contractsÂ’ maturity dates. As exchange rates change, gains and losses on these contracts are generated based on the change in the exchange rates that are recognized in the consolidated statement of operations at maturity, and offset the impact of the change in exchange rates on the foreign currency cash flows that are hedged. If the counterparties to the exchange contracts do not fulfill their obligations to deliver the contracted currencies, we could be at risk for currency related fluctuations. During January 2012, we entered into a foreign exchange, fixed interest rate swap contract that provides for us to pay a fixed interest rate on the underlying loan balance denominated in Chilean Pesos. We entered into this agreement in Chile for purchases of inventory denominated in U.S. dollars. A hypothetical 1% interest rate change or 10% foreign exchange rate change will not have a material impact on our results from operations or financial position. We enter into these contracts with counterparties that we believe to be creditworthy and do not enter into any leveraged derivative transactions. We had $3.2 million in foreign exchange forward contracts outstanding at MarchÌý31, 2012, primarily to hedge Chilean-based operating cash flows against US dollars. If Chilean Pesos were to strengthen in relation to the US dollar, our loss or gain on hedged foreign currency cash-flows would be offset by the derivative contracts, with a net effect of zero.

We do not engage in trading market risk sensitive instruments or purchasing hedging instruments or “other than trading” instruments that are likely to expose us to significant market risk, whether interest rate, foreign currency exchange, commodity price, or equity price risk.

Interest Rate Risk – Our exposure to market risk relates to our cash and investments and to our borrowings. We maintain an investment portfolio of money market funds. The securities in our investment portfolio are not leveraged, and are, due to their very short-term nature, subject to minimal interest rate risk. We currently do not hedge interest rate exposure. Because of the short-term maturities of our investments, we do not believe that a change in market interest rates would have a significant negative impact on the value of our investment portfolio except for reduced income in a low interest rate environment. At MarchÌý31, 2012, we had cash, cash equivalents and marketable securities of $62.1Ìýmillion. The weighted average interest rate related to our cash and cash equivalents for the three months ended MarchÌý31, 2012 was 0%. As of MarchÌý31, 2012, the principal value of our credit lines was $14.2Ìýmillion at a weighted average interest rate of approximately 7% for the three months then ended.

The primary objective of our investment activities is to preserve principal while at the same time maximizing yields without significantly increasing risk. To achieve this objective, we invest our excess cash in debt instruments of the U.S. Government and its agencies, bank obligations, repurchase agreements and high-quality corporate issuers, and money market funds that invest in such debt instruments, and, by policy, restrict our exposure to any single corporate issuer by imposing concentration limits. To minimize the exposure due to adverse shifts in interest rates, we maintain investments at an average maturity of generally less than three months.

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ItemÌý4. Controls and Procedures

The CompanyÂ’s management, under the supervision and with the participation of the CompanyÂ’s Chief Executive Officer (“CEO”) and Chief Financial Officer (“CFO”), has evaluated the effectiveness of the CompanyÂ’s disclosure controls and procedures as defined in Securities and Exchange Commission (“SEC”) RuleÌý13a-15(e) as of MarchÌý31, 2012. Based on that evaluation, the CEO and CFO have concluded that the CompanyÂ’s disclosure controls and procedures are effective to ensure that information the Company is required to disclose in reports that it files or submits under the Securities Exchange Act is accumulated and communicated to management, including the CEO and CFO, as appropriate, to allow timely decisions regarding required disclosure and is recorded, processed, summarized, and reported within the time periods specified in the SECÂ’s rules and forms.

Changes to the CompanyÂ’s Internal Control Over Financial Reporting

In connection with the closing of the FineTech acquisition in December 2011, we began implementing standards and procedures at FineTech including upgrading and establishing controls over accounting systems, and adding employees and consultants who are trained and experienced in the preparation of financial statements in accordance with U.S. GAAP to ensure that we have in place appropriate internal control over financial reporting at FineTech. Other than as set forth above with respect to FineTech, there have been no changes to the CompanyÂ’s internal control over financial reporting that occurred during the CompanyÂ’s first fiscal quarter of 2012 that have materially affected, or are reasonably likely to materially affect, the CompanyÂ’s internal control over financial reporting.

FineTechÂ’s assets constituted $36.3 million and $28.1 million of total and net assets, respectively, as of MarchÌý31, 2012 and $1.6 and $0.3 million of revenues and net loss, respectively, for the three months ended MarchÌý31, 2012.

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PART II. OTHER INFORMATION

ItemÌý1. Legal Proceedings

We are a party to litigation in the ordinary course of business. We do not believe that any such litigation will have a material adverse effect on our business, financial condition or results of operations.

ItemÌý1A. Risk Factors

There have been no material changes from the risk factors as previously disclosed in the ItemÌý1A of the Company Annual Report on Form 10-K.

ItemÌý2. Unregistered Sales of Equity Securities and Use of Proceeds

None.

ItemÌý3. Defaults Upon Senior Securities

None.

ItemÌý4. Mine Safety Disclosures

Not Applicable.

ItemÌý5. Other Information

None.

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ItemÌý6. Exhibits.

Ìý

Exhibit 2.7 Ìý Stock Purchase Agreement, dated JanuaryÌý20, 2012, by and among СÖíÊÓƵapp Health, Inc., СÖíÊÓƵapp Chile S.A., Samuel Alexandre Arama, Inversiones SVJV Limitada, Bruno Sergiani, Inversiones BS Limitada, Pierre-Yves Le Goff, and Inversiones PYTT Limitada.
ExhibitÌý3.1(1) Ìý Amended and Restated Certificate of Incorporation.
ExhibitÌý3.2(2) Ìý Amended and Restated By-Laws.
ExhibitÌý31.1 Ìý Certification by Phillip Frost, Chief Executive Officer, pursuant to RuleÌý13a-14(a) and 15d-14(a) of the Securities and Exchange Act of 1934 as adopted pursuant to SectionÌý302 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended MarchÌý31, 2012.
ExhibitÌý31.2 Ìý Certification by Rao Uppaluri, Chief Financial Officer, pursuant to RuleÌý13a-14(a) and 15d-14(a) of the Securities and Exchange Act of 1934 as adopted pursuant to SectionÌý302 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended MarchÌý31, 2012.
ExhibitÌý32.1 Ìý Certification by Phillip Frost, Chief Executive Officer pursuant to 18 U.S.C. SectionÌý1350, as adopted pursuant to SectionÌý906 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended MarchÌý31, 2012.
ExhibitÌý32.2 Ìý Certification by Rao Uppaluri, Chief Financial Officer pursuant to 18 U.S.C. SectionÌý1350, as adopted pursuant to SectionÌý906 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended MarchÌý31, 2012.
ExhibitÌý101* Ìý The following materials from the CompanyÂ’s Quarterly Report on Form 10-Q for the quarter ended MarchÌý31, 2012, formatted in XBRL (Extensible Business Reporting Language): (i) Condensed Consolidated Balance Sheets, (ii) Condensed Consolidated Statements of Operations, (iii) Condensed Consolidated Statements of Cash Flows, and (iv) Notes to Financial Statements, tagged as blocks of text.

Ìý

* As provided in Rule 406T of Regulation S-T, this information is furnished herewith and not filed for purposes of sections 11 and 12 of the Securities Act of 1933, as amended, or section 18 of the Securities Exchange Act of 1934, as amended.
(1)Ìý

Filed with the CompanyÂ’s Current Report on Form 8-A filed with the Securities and Exchange Commission on JuneÌý11, 2007, and incorporated herein by reference.

(2)Ìý

Filed with the CompanyÂ’s Annual Report on Form 10-K filed with the Securities and Exchange Commission on MarchÌý31, 2008, and incorporated herein by reference.

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SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

Ìý

Date: MayÌý10, 2012 Ìý Ìý СÖíÊÓƵapp Health, Inc.
Ìý Ìý Ìý

/s/ÌýAdam Logal

Ìý Ìý Ìý Adam Logal
Ìý Ìý Ìý Executive Director of Finance, Chief Accounting Officer and Treasurer

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Exhibit Index

Ìý

Exhibit
Number
ÌýÌý Description
ExhibitÌý2.7 ÌýÌý Stock Purchase Agreement, dated JanuaryÌý20, 2012, by and among СÖíÊÓƵapp Health, Inc., СÖíÊÓƵapp Chile S.A., Samuel Alexandre Arama, Inversiones SVJV Limitada, Bruno Sergiani, Inversiones BS Limitada, Pierre-Yves Le Goff, and Inversiones PYTT Limitada.
ExhibitÌý31.1 ÌýÌý Certification by Phillip Frost, Chief Executive Officer, pursuant to RuleÌý13a-14(a) and 15d-14(a) of the Securities and Exchange Act of 1934 as adopted pursuant to SectionÌý302 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended MarchÌý31, 2012.
ExhibitÌý31.2 ÌýÌý Certification by Rao Uppaluri, Chief Financial Officer, pursuant to RuleÌý13a-14(a) and 15d-14(a) of the Securities and Exchange Act of 1934 as adopted pursuant to SectionÌý302 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended MarchÌý31, 2012.
ExhibitÌý32.1 ÌýÌý Certification by Phillip Frost, Chief Executive Officer pursuant to 18 U.S.C. SectionÌý1350, as adopted pursuant to SectionÌý906 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended MarchÌý31, 2012.
ExhibitÌý32.2 ÌýÌý Certification by Rao Uppaluri, Chief Financial Officer pursuant to 18 U.S.C. SectionÌý1350, as adopted pursuant to SectionÌý906 of the Sarbanes-Oxley Act of 2002 for the quarterly period ended MarchÌý31, 2012.
ExhibitÌý101* ÌýÌý The following materials from the CompanyÂ’s Quarterly Report on Form 10-Q for the quarter ended MarchÌý31, 2012, formatted in XBRL (Extensible Business Reporting Language): (i) Condensed Consolidated Balance Sheets, (ii) Condensed Consolidated Statements of Operations, (iii) Condensed Consolidated Statements of Cash Flows, and (iv) Notes to Financial Statements, tagged as blocks of text.

Ìý

* As provided in Rule 406T of Regulation S-T, this information is furnished herewith and not filed for purposes of sections 11 and 12 of the Securities Act of 1933, as amended, or section 18 of the Securities Exchange Act of 1934, as amended.

Ìý

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