New test that helps identify HCV in blood receives FDA approval

Roche, a pharmaceutical company, announced that the U.S. Food and Drug Administration approved the cobas TaqScreen MPX Test, v2.0.

The test can be used in the detection and identification of HIV, Hepatitis C virus and Hepatitis B virus in human blood. This is the latest version of the cobas TaqScreen MPX Test and it provides increased sensitivity. It uses real-time, multi-dye PCR technology to detect and discriminate for HIV, HCV and HBV.

The test has received the CE Mark and has been approved in Canada, Brazil, China and India.  

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