Chembio Diagnostics, Inc. Files For CLIA Waiver With FDA For Point-Of-Care DPP(R) HIV 1/2 Assay

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MEDFORD, N.Y., Dec. 2, 2013 (GLOBE NEWSWIRE) -- Chembio Diagnostics, Inc. (Nasdaq:CEMI), a leader in point-of-care (“POC”) diagnostic tests for infectious diseases, has completed its Clinical Laboratory Improvement Amendment (“CLIA”) waiver studies for its DPP® HIV 1/2 Assay (the “Assay”). The Company believes the study results meet CLIA waiver requirements and it has filed the CLIA waiver application with the U.S. Food and Drug Administration (“FDA”).

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