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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

April 28, 2014

View Archived Issues

FDA approves first HPV test for primary cervical cancer screening

The FDA has approved the cobas HPV (human papillomavirus) test from Roche (Basel, Switzerland) as a first-line primary screening test for cervical cancer in women 25 and older. The approval follows the March 12 unanimous recommendation from the Microbiology Devices Panel of the FDA's Medical Devices Advisory Committee, making the cobas the only HPV test in the U.S. approved for first-line primary screening. Previously HPV tests had been used as a follow-up test for Pap (Papanicolaou) results and as an adjunct to Pap in women over 30. Read More

Come on Over!: Neural prosthesis doubles as an electroporation device

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FDLI Annual Meeting: Consultant: Interest in companion Dx 'waning,' says payers skeptical

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Washington Roundup: FDA post-market draft hints at lengthier post-approval studies

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MDD's Stock Watch

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Financings Roundup: Lombard to offer 5 million shares at $11/per in IPO

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Agreements/contracts: Escalon to distribute BiCOM's transpalpebral tonometer

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People in Places

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Product briefs

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MDD's Neurology Extra

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