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BioWorld - Friday, May 22, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Sep. 16, 2015

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Veracyte Continues to build case for Afirma: Afirma's effectiveness affirmed through independent study results

Obtaining FDA approval for a product doesn't mean a company can rest on its laurels. In many cases, the work is really just beginning said Veracyte's (South San Francisco) President/CEO Bonnie Anderson. After approval comes the process of compiling a compelling body of post market data to help drive adoption rates. Nearly four years after obtaining FDA approval for the Afirma gene expression classifer (GEC), a test that is able to identify patients, whose thyroid nodules are noncancerous, Veracyte is in the process of garnering data. Read More

Inside the Beltway: Authors argue ACOs failing to prove themselves as cost savers

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Looking to repeat Pharma successes in Med-Tech: China is rapidly transforming itself into major player in medical technology space

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Inner-ear Chaos: UCLA team develops alternative to craniotomy for rare condition

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Daily M&A: Erba Diagnostics Mannheim completes Lumora acquisition

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Agreements/contracts: Seegene, BD to develop molecular diagnostic assays

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Patent Watch: Therasolve receives U.S. patent for MemoPatch reminder technology

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MDD's Oncology Extra

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