SOURCE: Chembio Diagnostics, Inc.

Chembio Diagnostics, Inc.

March 03, 2011 08:00 ET

Chembio Reports Record Annual & Quarterly Results

Conference Call Scheduled for Thursday, March 3, 2011, at 10:00 a.m. Eastern Time

MEDFORD, NY--(Marketwire - March 3, 2011) - Chembio Diagnostics, Inc. (OTCQB: CEMI) (PINKSHEETS: CEMI), which develops, manufactures, markets and licenses point-of-care diagnostic tests, reported record revenues and earnings for the year ended December 31, 2010. Total revenues were $16.7 million for the year ended December 31, 2010, which compares to total revenues of $13.8 million for the year ended December 31, 2009, a 20.8% increase. The Company recorded net income of approximately $2.51 million, or $0.04 per share, for the year ended December 31, 2010, compared to net income of approximately $309,000, or less than $0.01 per share, for the year ended December 31, 2009. Total revenues were $5.67 million for the three months ended December 31, 2010, which compares to total revenues of $3.55 million for the three months ended December 31, 2009, a 60% increase. The Company recorded net income of approximately $1.88 million, or $0.03 per share, for the three months ended December 31, 2010, compared to a net income of approximately $217,000, or less than $0.01 per share, for the three months ended December 31, 2009.

The Company realized a record amount of revenues related to research & development milestones and grants, which increased 106% to $2.76 million in the year ended December 31, 2010 from $1.34 million in the year ended December 31 2009. Also contributing to the record revenues was an 83% increase in sales of the Company's rapid HIV tests to customers in Africa where its products are used in national testing programs principally funded by the U.S. President's Emergency Plan for AIDS Relief ("PEPFAR") and/or the Global Fund to Fight AIDS, Tuberculosis & Malaria. The Company's 2010 DPP® product sales were $.63 million, level with 2009. However all of the 2009 DPP® product sales were for evaluations and regulatory submissions undertaken by FIOCRUZ, the Company's OEM customer in Brazil; most of the 2010 sales were the initial sales of product that would be used in a new national testing protocol being considered in Brazil.

The operating results in 2010 include $5.28 million of revenues from the sale of rapid HIV tests to Alere, Inc. ("Alere" formerly Inverness Medical Innovations, Inc.), the Company's exclusive U.S. marketing partner for its two FDA approved rapid HIV tests. This represents an increase of $40,000, or less than 1%, compared to $5.24 million for the year ended December 31, 2009. Sales to Alere in the fourth quarter of 2010 were $1.74 million, a decrease of $93,000 or 5% as compared to the fourth quarter in 2009. During 2010 we believe Alere increased its sales of our products by at least 25%, however due to inventory level changes at Alere, this is not reflected in our results. During 2010 we also completed paying the $1.01 million liability to Alere that we incurred in 2008, which will enhance our future cash flows.

The 2010 operating results include $1.47 million in Qualified Therapeutic Discovery Project grants ("QTDP") under Section 48D of the Internal Revenue Code, as enacted under the Patient Protection and Affordable Care Act of 2010. This amount was reflected as a reduction of research and development expenses (R&D).

The operating results also included approximately $275,000 of expenses incurred in connection with two specific potential strategic opportunities, including approximately $100,000 for legal fees, including patent research and due diligence, $100,000 for outside directors' Special Committee fees, $37,500 for a valuation consultant deposit, $25,000 for investment consulting fees and $12,500 in various other expenses. One of these potential opportunities, which was unsolicited, involved due diligence, travel and negotiation, and preparation of a written agreement which was not finalized, and the other involved travel and extensive negotiations and due diligence. Both opportunities involved numerous meetings, conferences and discussions by and with management, Chembio's outside directors and counsel, both for internal strategy sessions and with the proposed strategic partner. Neither of the potential opportunities ultimately resulted in any material agreement. The Company's senior management and board believes strongly in the value that has been created and the opportunities there are for further increasing shareholder value, particularly once it begins to commercialize the products in its development and clinical pipeline. Chembio continues to consider strategic opportunities that it believes are attractive. Finally, we expended approximately $650,000 of clinical trial expenses in 2010 related to our oral fluid HIV test PMA, including $253,000 in the fourth quarter.

The $275,000 in strategic investigation costs in SG&A expenses, $1.467 million QTDP benefit (expense reduction), and the $650,000 clinical trial expense each had a material impact on our 2010 net income.

Commenting on the results, Chembio's President, Lawrence A. Siebert, stated, "We are very pleased with our 2010 results, which included strong growth in our base business of lateral flow HIV tests, and record revenue from research and development contracts and grants, all of which enabled us to increase our investment in our new and growing DPP® product pipeline. I believe we are very well positioned to deliver continued growth in 2011 and beyond, as the growth from our base business is accelerated from the commercialization of our new DPP® rapid, point-of-care products. We believe that our strategy of developing a core public health brand, initially with our DPP® HIV Oral Fluid HIV test and our DPP® Syphilis Screen & Confirm test, and of complementing this business with OEM opportunities in all other market segments, is sound and will continue."

Financial Highlights for 2010

-- Product sales for the year ended December 31, 2010 increased 9% to a
   record $13.52 million from $12.37 million in 2009, which was the
   Company's previous record for revenues. Net product sales to Alere for
   the year remained steady, as compared with the year of 2009.

-- Product sales also included the shipment of HIV rapid tests and
   components to customers in Africa ($6.13MM), South America ($1.05MM),
   and Asia, Europe, and the Middle East ($.36MM).

-- Also included in our 2010 product sales was $628,100 of DPP® product
   sales, an increase of 1%, or $8,600, as compared to $619,500 in 2009.
   These sales were for two of the four DPP® products we contracted for
   In 2008 with our Brazilian customer FIOCRUZ. Approximately $84,000 of
   these sales reflect products provided FIOCRUZ' to submit product for
   evaluation, laboratory and field studies, and regulatory approval. The
   balance was for the DPP® HIV 1/2 Screen test. Delays have occurred in
   FIOCRUZ obtaining certain other regulatory approvals, although we
   believe that these regulatory approvals will be achieved during the
   first and/or second quarters of 2011.

-- The increased product and R&D, milestone and grant revenues combined
   to produce gross margin dollars that were $2.24 million, or 38%,
   greater ($8.10 million vs. $5.86 million) in 2010 than the gross
   margin dollars in 2009.

-- Research and development expenses, excluding the effect of the QTDP
   grants, increased by $1.17 million, or 41%, to $4.05 million compared
   to $2.88 million in the 2009 period. The QTDP grant reduced research
   and development expenses in 2010 to $2.59 million. The Company has
   nevertheless over the same period increased its research & development
   expenses, as more products based on the Company's patented DPP®
   technology were validated for manufacture and entered the clinical
   evaluation and regulatory approval process.

-- The operating results also include approximately $654,000 of clinical
   trials expenses ongoing in support of an FDA Pre-Marketing Approval
   ("PMA") related to its DPP® HIV 1/2 screening test for use with oral
   fluid or blood samples.

-- Selling General & Administrative Expenses increased by $281,000, or
   10.6%, in the year of 2010 as compared to the year of 2009. This was
   primarily due to the recording of $94,000 in Brazilian tax withholdings
   on the milestone payments and an increase in investor relations.

-- Operating income was approximately $2.57 million in 2010 as compared to
   operating income in 2009 of $.32 million, an increase of $2.25 million.
   In addition, net income was approximately $2.51 million in 2010 as
   compared to net income in 2009 of $309,000, an increase of $2.20
   million.

-- The December 31, 2010 cash balance was $1.07 million more than as of
   December 31, 2009. This was primarily due to $1.02 million in cash
   provided from operations. Also contributing to the cash increase was
   a $250,000 term loan from HSBC. Partially offsetting these cash inflows
   was our investment in fixed assets.

Financial Highlights for the Quarter ended December 31, 2010

-- Product sales for the quarter ended December 31, 2010 (fourth quarter)
   increased 65.6% to $5.18 million from $3.13 million in the same period
   of 2009.

-- R&D revenues for the fourth quarter increased $70,000 to $456,000 from
   $386,000 in the same period of 2009

-- The increased product and R&D revenues in the fourth quarter of 2010,
   together with the effect of the QTDP grants, combined to produce gross
   margin dollars that were $.86 million, or 53%, greater ($2.51 million
   vs. $1.63 million) than the gross margin dollars in the comparable
   period in 2009.

-- Research and development expenses, excluding the effect of the QTDP
   grants, increased by $.48 million or 63% to $1.23 million compared to
   $.76 million in the 2009 period. The QTDP grants reduced research and
   development expenses to $(.24) million in the 2010 period.

-- Selling General & Administrative Expenses increased by $140,000 or 21%
   in the fourth quarter of 2010 as compared to the fourth quarter of
   2009. This was primarily due to an increase in commissions for the
   increased sales made to Brazil of our DPP® products.

-- Operating profit was approximately $1.93 million, in the fourth quarter
   of 2010 as compared to operating income in the fourth quarter of 2009
   of $218,000, an increase of $1.71 million. In addition, net income was
   approximately $1.88 million in the fourth quarter of 2010 as compared
   to net income in the fourth quarter of 2009 of $217,000, an increase of
   $1.66 million. The QTDP grants had a significant impact upon both
   operating profit and net income for the fourth quarter of 2010.

Information Concerning the Market for our Common Stock

On February 24, 2011, and since that date, our stock has not been quoted on the OTC Bulletin Board, and is now being quoted on the OTCQB, which is the second of the three tiers of the OTC Market Group. The situation is in a state of flux and we are trying to determine what market we believe is best for our stock, considering the relative costs, liquidity, market strategy, etc. The other markets that we will consider are (1) the higher tier of the OTC Market Group called OTC-QX; (2) the NYSE-AMEX, and; (3) NASDAQ. Our stock is no longer trading on the OTC Bulletin Board because the market maker that had filed originally to quote our stock on the OTC Bulletin Board is no longer providing quotes on the OTC Bulletin Board. It is our understanding that a large number of other market makers also have ceased to provide quotes on the OTC Bulletin Board and that 300 to 500 other companies have ceased being quoted on the OTC Bulletin Board during the past few months for the same reason.

This change has nothing to do with Chembio or the quality of our company. It is solely related to the desire of the market makers to save costs related to providing quotes on the OTC Bulletin Board.

Certain third-party stock data providers such as Yahoo Finance are still in the process of updating their platforms to correctly display the trading activity of companies that have transitioned from OTCBB to OTCQB. For price and volume information regarding Chembio on the OTCQB marketplace please visit: http://www.otcmarkets.com/stock/CEMI/quote

Summary of R&D, Clinical and Commercialization Programs

-- DPP® HIV Oral Fluid Screening Assay - During 2010 we made significant
   progress toward commercializing this product globally, as follows.
   -- FDA PMA Application Status - We commenced clinical trials in the
      United States in support of a planned Pre-Marketing Approval (PMA)
      application to the FDA. We have enrolled about half of the 3,000
      patients in the clinical protocol and we are on a schedule for
      completing this clinical trial this summer. We recently submitted a
      request to file a modular PMA to the FDA which allows us to submit
      our preclinical data and manufacturing information for review while
      still collecting, compiling and analyzing clinical data. The first,
      second and third modules are being planned for submission to FDA in
      the first, second and third quarters, respectively.
   -- International Market - In March we obtained approval of this product
      from the United States PEPFAR program, and reported the results of
      studies done in Mozambique and Nigeria supporting this approval
      which demonstrating excellent performance of this product. We are
      submitting this product for inclusion in the WHO procurement list as
      well.
-- DPP® Syphilis Screen & Confirm Test -
   -- US FDA Clearance - We are completing the internal processes necessary
      to commence clinical studies for the products in the United States.
      Clinical studies are being scheduled for 2nd Quarter of this year to
      support the FDA pre-market clearance (510k). A study we conducted in
      collaboration with the CDC that was published in December in the
      Journal of Clinical Microbiology, as well as studies reported by CDC
      confirm the value of our multiplex DPP® Syphilis Screen & Confirm
      test.
   -- China Evaluation - Through our ongoing collaboration with the CDC for
      this product, we were invited by the WHO Collaborating Center in
      China to conduct a training session there in January for a multi-site
      evaluation of this product which is starting now and that is
      scheduled to be completed during the second quarter. Our DPP®
      patent was just issued in China, where syphilis is on the rise, and
      we have begun to consider various opportunities for distribution and
      manufacturing of our products there, including but not limited to
      this product.
   -- CE Mark - When we are ready to begin the clinical studies for this
      product we will alos be able to submit this product for
      self-certification of a CE Mark, which submission we anticipate
      filing in the 2nd quarter 2011.

-- FIOCRUZ Programs - We have five active projects with FIOCRUZ, four
   relating to agreements signed in 2008 and one (Syphilis) signed in
   2010.
   -- Approval of DPP® HIV Screening and Confirmatory Assays - During
      2010 ANVISA granted FIOCRUZ approval to market our DPP® HIV 1/2
      Screening and Confirmatory Tests. We believe the Ministry of
      Health in Brazil is seeking to have these products used in a new
      serial testing algorithm to be deployed nationally, and that an
      evaluation concerning this new algorithm is ongoing.
   -- DPP® Canine Leishmaniasis - In January 2011 FIOCRUZ was requested
      by MAPA for the second time to provide additional information.
      This will further delay the approval process and based upon recent
      experience it is difficult to predict timing. Nevertheless, based
      on our discussions with FIOCRUZ, we believe there remains strong
      support for this product within FIOCRUZ and that they are
      continuing their efforts in prosecuting the approval of this product
      by MAPA.
   -- DPP® Leptospirosis - Chembio sent three production lots of this
      product to FIOCRUZ and FIOCRUZ is completing the preparation of a
      technical file in order to submit to ANVISA for approval. FIOCRUZ
      estimates ANVISA approval will be granted during the second quarter
      of 2011.
   -- DPP® Syphilis Treponemal - Chembio sent three production lots of to
      FIOCRUZ and FIOCRUZ is completing the preparation of a technical
      file in order to submit to ANVISA for approval. FIOCRUZ estimates
      ANVISA approval will be granted during the second quarter of 2011.

We also had significant progress on the following projects in 2010

-- Bio-Rad Laboratories OEM Multiplex DPP® Agreement - In June 2010
   Bio-Rad confirmed that the product development activity had been
   completed in accordance with the agreed-upon specifications,
   resulting in a license fee being earned. At that time Bio-Rad also
   exercised its option to have Chembio transfer the manufacturing of
   this product to Bio-Rad, which process was also satisfactorily
   completed, in October 2010, resulting in additional agreed-upon
   fees being earned. We believe that Bio-Rad will begin to market
   this product in Europe beginning in 2012, and in the United States
   in 2013, although there can be no assurance of this. During 2010,
   Chembio earned approximately $128,000 for product development work
   rendered to Bio-Rad under this agreement, plus an additional $615,000
   in license and other fees related to the manufacturing transfer.

-- Battelle/CDC DPP® Multiplex Influenza Immunity Test - In
   December 2009 Chembio entered into a milestone-based development
   agreement for the development and initial supply of a multiplex,
   rapid point-of-care ("POC") influenza immunity test. During 2010
   development work with respect to the contract development
   specification was substantially completed. Our contract partners are
   assessing the prototype product and determining potential additional
   funded development activity. During 2010, Chembio earned approximately
   $804,000 in milestones for product development work rendered under
   this agreement.

-- DPP® Influenza - We have developed a prototype multiplex test for
   FLU A/B Antigen Detection and plan to complete R&D development for
   this test in March 2011 and to complete validation by the end of the
   second quarter of 2011. We will submit our pre-IDE to 510K in July 2011
   based on our current plan. This will help us to conduct clinical trials
   during late 2011 and/or early 2012.

-- DPP® Leptospirosis Phase II Grant - In 2009 we were awarded a three
   year, $1.9 million Small Business Innovative Research (SBIR) Phase II
   grant from the United States National Institutes of Health (NIH) to
   fully develop, validate, and commercialize a rapid diagnostic test for
   Leptospirosis for general use worldwide, and our work is progressing
   on schedule. To date, we have identified several novel leptospiral
   proteins cloned from a variety of strains that are prevalent in
   different countries. These antigens will supplement the current test
   prototype and thus enhance the potential for its use worldwide as a
   universal point-of-care test for leptospirosis.

-- DPP® Tuberculosis Phase II Grant - In February 2011 we were awarded
   an SBIR Phase II grant from the NIH to continue development of a simple,
   rapid, accurate, and cost-effective serological test for active
   tuberculosis that can be utilized in resource-limited settings.
   Chembio developed a prototype of this test in the Phase I work in
   collaboration with the Infectious Disease Research Institute ("IDRI"),
   a Seattle-based biotechnology research organization dedicated to
   technologies that address diseases in the developing world; this
   collaboration will continue in this second phase of the research and
   development grant as well. The grant is effective March 1, 2011. The
   prototype test developed during the Phase I work uses the Dual Path
   Platform (DPP®) technology together with selected antigens from a
   large panel of novel recombinant antigens identified at IDRI. The
   Phase I studies demonstrated the feasibility of developing a rapid
   and accurate test for tuberculosis with required diagnostic
   performance characteristics (sensitivity > 80%, specificity > 95%).
   In Phase II, the proposed rapid (15 minutes) point-of-care DPP® test
   for tuberculosis will be fully developed, optimized, and evaluated
   in multi-center clinical trials in several countries, followed by
   validation of production protocols, preparation for regulatory
   approval and commercialization

-- DPP® Hepatitis C - In 2010 we received data from a study sponsored by
   the CDC that assessed the performance of our HCV product. The data,
   which we believe will be published soon, confirmed that we had
   achieved good performance with this HCV antibody detection test
   prototype. We have recently been invited to participate in some
   additional CDC studies this year with this and certain other
   related prototype products that we have in development in this
   area. We have also determined however that the market opportunity
   for a point of care HCV antibody only (i.e., without antigen detection)
   test is very limited, and so in addition to improving our antibody
   detection test, we are also working on including antigen detection as
   well as in a new DPP® format that we have in development, which format
   incorporates some of our platform enhancements (see below). We believe
   this could result in a more commercially viable market opportunity for
   this market.

Other Activities & Developments

-- Platform Enhancements - During 2010 and increasingly during 2011
   we are improving and enhancing the capabilities of our DPP®
   technology. For example, we are further simplifying the procedure
   to run certain kinds of tests developed with DPP® and we are also
   making antibody and antigen detection available in a single test
   device without certain limitations that exist when this is attempted
   with lateral flow technology.

-- Operations - We have also fully integrated the new automated assembly
   system into our manufacturing operation, which will make all of our
   production, both lateral flow and DPP®, more cost effective.

-- Patents Issued & Pending - The Company has obtained patent coverage on
   the DPP® product line, including three U.S. patents, and patents in
   China, Malaysia, Eurasia, Mexico, Singapore, and the U.K. Additional
   patents applications on the DPP® product line are pending in the U.S.,
   as well as in many foreign countries such as Australia, Brazil, Canada,
   the European Union, India, Indonesia, Israel, Japan, Korea, and
   South Africa. Patents have also been filed on extensions to the DPP®
   product line concept.

There can be no assurance that any of these projects will continue, meet regulatory or other technical requirements and specifications, and/or that if continued, will result in completed products, or that such products, if successfully completed, will be successfully commercialized.

Conference Call

Chembio has scheduled a conference call and webcast for 10:00 a.m. Eastern time on Thursday, March 3, 2011. To participate on the conference call, please dial (877) 407-0778 from the U.S. or (201) 689-8565 from outside the U.S. In addition, following the completion of the call, a telephone replay will be accessible until March 10, 2011 at 11:59 p.m. Eastern Time by dialing (877) 660-6853 from the U.S. or (201) 612-7415 from outside the U.S. and entering reservation account number 286 and conference ID #: 36779. The conference call may also be accessed via the internet at http://www.investorcalendar.com/IC/CEPage.asp?ID=163520. An archive of the webcast will be available for 90 days on the Company's website at www.chembio.com.

Investor Presentation

The Company has prepared and filed a new investor presentation. It can be accessed through the following link: http://phx.corporate-ir.net/phoenix.zhtml?c=121584&p=irol-IRhome.

About Chembio Diagnostics

Chembio Diagnostics, Inc. develops, manufactures, licenses and markets proprietary rapid diagnostic tests in the growing $7 billion point-of-care testing market. Chembio's two FDA PMA-approved, CLIA-waived, rapid HIV tests are marketed in the U.S. by Inverness Medical Innovations, Inc. Chembio markets its HIV STAT-PAK® line of rapid HIV tests internationally to government and donor-funded programs directly and through distributors. Chembio has developed a patented point-of-care test platform technology, the Dual Path Platform (DPP®) technology, which has significant advantages over lateral-flow technologies. This technology is providing Chembio with a significant pipeline of business opportunities for the development and manufacture of new products based on DPP®. Headquartered in Medford, NY, with approximately 100 employees, Chembio is licensed by the U.S. Food and Drug Administration (FDA) as well as the U. S. Department of Agriculture (USDA), and is certified for the global market under the International Standards Organization (ISO) directive 13.485.

Forward-Looking Statements

Statements contained herein that are not historical facts may be forward-looking statements within the meaning of the Securities Act of 1933, as amended. Forward-looking statements include statements regarding the intent, belief or current expectations of the Company and its management. Such statements are estimates only, as the Company has not completed the preparation of its financial statements for those periods, nor has its auditor completed a review or audit of those results. Actual revenue may differ materially from those anticipated in this press release. Such statements reflect management's current views, are based on certain assumptions and involve risks and uncertainties. Actual results, events, or performance may differ materially from the above forward-looking statements due to a number of important factors, and will be dependent upon a variety of factors, including, but not limited to Chembio's ability to obtain additional financing, to obtain regulatory approvals in a timely manner and the demand for Chembio's products. Chembio undertakes no obligation to publicly update these forward-looking statements to reflect events or circumstances that occur after the date hereof or to reflect any change in Chembio's expectations with regard to these forward-looking statements or the occurrence of unanticipated events. Factors that may impact Chembio's success are more fully disclosed in Chembio's most recent public filings with the U.S. Securities and Exchange Commission.

(Tables to follow)


                        Chembio Diagnostics, Inc.
                     Summary of Results of Operations

                              For the
                        three months ended
                            (Unaudited)             For the years ended
                     -------------------------   --------------------------
                     December 31,  December 31,  December 31,  December 31,
                         2010          2009          2010          2009
                     ------------  ------------  ------------  ------------
Net product sales    $  5,179,226  $  3,127,454  $ 13,516,359  $ 12,372,493

License and royalty
 revenue                   31,480        38,186       432,238       121,896

R&D, milestone and
 grant revenue            456,136       385,801     2,756,106     1,339,859
                     ------------  ------------  ------------  ------------

Total Revenues       $  5,666,842  $  3,551,441  $ 16,704,703  $ 13,834,248

Gross Profit         $  2,490,858  $  1,630,805  $  8,100,699  $  5,860,405

Research and
 development
 expenses            $   (236,147) $    755,837  $  2,586,308  $  2,883,696

Selling, general and
 administrative
 expenses            $    797,006  $    657,309  $  2,940,721  $  2,659,382

Income from
 operations          $  1,929,999  $    217,659  $  2,573,670  $    317,327

Net income           $  1,880,776  $    217,214  $  2,513,344  $    309,060

Basic earnings
 per share           $       0.03  $       0.00  $       0.04  $       0.00

Diluted earnings
 per share           $       0.03  $       0.00  $       0.04  $       0.00

Weighted average
 number of shares
 outstanding, basic    62,204,742    61,950,988    62,102,861    61,946,435

Weighted average
 number of shares
 outstanding,
 diluted               70,513,280    75,365,550    70,920,915    75,041,932





                        Chembio Diagnostics, Inc.
                        Summary of Balance Sheets

                                                December 31,  December 31,
                                                    2010          2009
                                                ------------  ------------

CURRENT ASSETS:
Cash                                            $  2,136,351  $  1,068,235
Accounts receivable, net of allowances             3,946,398     1,776,327
Inventories                                        1,349,161     1,555,903
Other current assets                                 204,824       266,637
                                                ------------  ------------
TOTAL CURRENT ASSETS                               7,636,734     4,667,102

NET FIXED ASSETS                                     813,214       580,213

OTHER ASSETS
Deposits on manufacturing equipment                        -       338,375
License agreements and other assets                  636,226       729,560
                                                ------------  ------------

                                                $  9,086,174  $  6,315,250
                                                ============  ============

TOTAL CURRENT LIABILITIES                       $  3,076,457  $  3,173,132

TOTAL OTHER LIABILITIES                              200,773        54,204
                                                ------------  ------------

TOTAL LIABILITIES                                  3,277,230     3,227,336

TOTAL STOCKHOLDERS' EQUITY                         5,808,944     3,087,914
                                                ------------  ------------

                                                $  9,086,174  $  6,315,250
                                                ============  ============





                        Chembio Diagnostics, Inc.
                           Summary of Cash Flow

                                                   For the years ended
                                                       (Unaudited)
                                                --------------------------
                                                December 31,  December 31,
                                                    2010          2009
                                                ------------  ------------

Net cash provided by operating activities       $  1,016,850  $    251,927
Net cash used in investing activities               (182,292)     (376,988)
Net cash provided by financing activities            233,558       (18,926)
                                                ------------  ------------
Net increase in cash and cash equivalents       $  1,113,939  $   (143,987)
                                                ============  ============

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