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美國Chembio Diagnostic Systems, Inc.
Chembio成立于1985年，開發(fā)、生產(chǎn)和銷售用于檢測傳染病的即時診斷檢驗方法和技術(shù)，并對其進行授權(quán)。通過推出其雙通道平臺(Dual Path Platform, DPP?)，Chembio開發(fā)了與口服液或血樣一起使用的DPP?口腔HIV 1&2篩選檢驗方法，這是全球市場上的第二種口腔HIV檢驗方法。

Chembio Diagnostic Systems, Inc. (OTCBB: CEMI) develops, manufactures, licenses and markets point-of-care (POC) diagnostic tests and technology for the detection of infectious diseases. Founded in 1985, Chembio entered the POC testing field in the late 1990’s and, in 2002, focused its business to participate in the emerging global need and opportunity for rapid HIV tests. As a result of this focus during the next six years, from 2003 through 2009, Chembio's total revenues grew at a compounded annual growth rate exceeding 30%, approaching $14MM in 2009. During 2009, Chembio's sales of its rapid HIV tests for the U.S. market through its U.S. marketing partner, Inverness Medical, increased 148% to $5.3MM.

Chembio’s Dual Path Platform (DPP?) POC technology was awarded United States Patent No. 7,189,522 in March 2007. DPP? enables development of POC assays that provide unique features and capabilities such as multiplexing and improved control of challenging sample types, such as oral fluid. Several new tests have already been developed on DPP? including a new oral fluid HIV 1/2 test, a new five-band POC confirmatory test for HIV 1/2, and a combination screening and confirmation test for Syphilis. Prototypes of an oral fluid test for Hepatitis C and various strains of influenza have also been developed.

Chembio is therefore now positioned to participate in the broader growing global market for POC diagnostic testing with this patented technology. The demand for point of care diagnostic products is increasing as a way to improve prevention efforts and thereby lower the costs of health care through earlier, easier and faster diagnosis. Our products serve diverse markets that are global.

All of Chembio’s activities are conducted by its approximately 100 employees from a 20,000 square foot leased facility in Medford (Long Island), NY, approximately one hour east of New York City and 15 minutes from Long Island’s MacArthur Airport. The facility is registered with both the United States Food and Drug Administration (FDA) and the United States Department of Agriculture (USDA). Chembio’s products are designed and manufactured in accordance with these agencies’ relevant quality standards as well as ISO-13.485. In 2004 Chembio registered its shares with the Securities and Exchange Commission, and its common stock trades on the Over-the-Counter Bulletin Board under the symbol CEMI.

Chembio’s core strengths are in its research, development, quality control, and manufacturing expertise. In certain instances partnerships are developed with leading marketing organizations for the exclusive development by Chembio, and the exclusive commercialization and distribution by our partner, of products developed pursuant to our customer’s OEM specifications.

Chembio’s HIV tests have been selected in the national testing protocols of several countries in Africa, Asia and Latin America. International relief efforts, led by the President’s Emergency Plan for Aids Relief (PEPFAR) and the UN Global Fund to Stop HIV, TB and Malaria (the Global Fund), have made significant strides toward prevention and treatment of HIV/AIDS, for which rapid HIV tests are an essential component.

In 2007, Chembio entered the United States rapid HIV test market. The Company’s two HIV tests that are FDA approved are based on lateral flow technology and are marketed exclusively in the U.S. by Inverness Medical Innovations, Inc. under their Clearview? brand as HIV 1/2 STAT-PAK? and COMPLETE HIV 1/2. In 2006 the United States Centers for Disease Control (CDC) revised their HIV testing guidelines by greatly expanding the recommended patient population for routine HIV testing in the U.S.. These recommendations are being adopted and implemented nationwide. Chembio is participating in this market expansion through its HIV tests that are marketed by Inverness.

Chembio is a party to several grants and other funded contract research and development agreements with entities that have included the United States National Institutes of Health (NIH), the CDC, the Foundation for Innovative and Novel Diagnostics (FIND), and the Infectious Disease Research Institute (IDRI). Work with these organizations involves efforts to develop rapid POC tests, all on DPP?, for Tuberculosis, Malaria, Leprosy, Leishmaniasis, Leptospirosis, Syphilis, HIV, Influenza, Hepatitis C, and other conditions in humans and animals. In each instance there is a demonstrated need for a simple, accurate, cost effective rapid diagnosis at the point of care.

Chembio has a new oral fluid HIV test which it developed with its DPP? technology. International evaluations are ongoing and clinical trials for U.S. market approval are expected to begin during 2009 and continue in 2010. Also, Chembio has a Cooperative Research & Development Agreement (CRADA) with the CDC to develop the world’s first rapid, POC combination screening and confirmatory test for Syphilis. This test, DPP? Syphilis Screen & Confirm, uniquely combines two markers on a single test strip which will enable a clinician to differentiate active versus past syphilis infection from a single finger-stick whole blood sample within 20 minutes. This will enable treatment decisions to occur at the POC. Development of the syphilis test is completed and several field and other studies are scheduled in the U.S. and globally during 2009 and 2010.

Chembio also has the unique experience in completing and executing technology transfer, agreements in the international market for rapid tests. These agreements ensure a cost effective means of providing local public health programs with needed POC screening and confirmatory tests by transferring know-how for the products that will ultimately be manufactured locally by Chembio’s customer. At the same time, these agreements provide qualified public and private entities with the ability to effectively address local conditions. To date, Chembio has concluded five such agreements with Bio-Manguinhos, an agency that is part of the Oswaldo Cruz Foundation and that is affiliated with the Brazilian Ministry of Health; other such agreements are in discussion for this and other markets.

Chembio believes strongly that its DPP? technology combined with its core competencies will enable the development of many next-generation rapid tests. The technology is available for applications in diverse global diagnostic markets for human and veterinary assays, food safety, bioterrorism, and environmental testing.