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Roche gets FDA okay for its Cobas TaqMan HBV test

tmcnet.com
Sep 6, 2008
        
Story Timeline:  127 days

Roche gets FDA okay for its Cobas TaqMan HBV test A Medical Device Daily Staff Report Roche Molecular Diagnostics (Pleasanton, California) reported FDA approval of the Roche Cobas TaqMan HBV Test, which the company said is the first assay for quantitating hepatitis B virus DNA to be approved in the U.S. The test uses Roche's real-time polymerase chain reaction (PCR) technology to quantify the amount of hepatitis... [read full story]                    

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Latest article on this story:

Roche gets FDA okay for its Cobas TaqMan HBV test

 pharmiweb.co.uk Sep 6, 2008
First article on this story:

FDA Approves First Hepatitis B Viral Load Test

 prnewswire.com Sep 4, 2008
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FDA Approves First Hepatitis B Viral Load Test

prnewswire.com
Sep 4, 2008
        

Another Roche first in TaqMan(R) real-time PCR testing for the diagnostic lab PLEASANTON, Calif., Sept. 4 /PRNewswire/ -- The U.S. Food & Drug Administration (FDA) has approved the Roche COBAS(R) TaqMan(R) HBV Test, the...