BETHLEHEM, Pa., March 23, 2011 (GLOBE NEWSWIRE) -- OraSure Technologies, Inc. (Nasdaq:OSUR) announced today that it has submitted to the U.S. Food and Drug Administration (“FDA”) an application for a waiver under the Clinical Laboratory Improvement Amendments of 1988 (“CLIA”) for its OraQuick® HCV Rapid Antibody Test for use with venous whole blood and fingerstick whole blood specimens.
