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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Feb. 25, 2013

View Archived Issues

SEMDA 2013: Shuren says FDA addressing concerns with review process

ATLANTA — For years medical device makers have fired off concerns and criticisms of the FDA's regulatory process – at times going so far as to call it unpredictable. Last week, during the Southeastern Medical Device Association's (SEMDA; Norcross, Georgia) annual conference held at the Georgia Institute of Technology Global Learning Center (Atlanta), med-tech firms got the chance to hear directly from the Center for Devices and Radiological Health's (CDRH) director – Jeffrey Shuren. Read More

State of the Spine Industry: Evolution, fusion, and PODs head the list of concerns

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Forget optimism, worldwide pressures continue in 2013

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Washington roundup: FDA releases draft guidance on recall versus enhancement

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Report from Europe: NxStage Medical gets CE mark for nocturnal home dialysis use

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Deals roundup: McKesson completes $2.1 billion acquisition of PSS World Medical

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Grants roundup: Palmetto Project gets support from AstraZeneca Foundation

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Agreements roundup: Vitas and Hospice Pharmacia enter three-year agreement

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Financings roundup: Celsion reports the sale of $15 million of its securities

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HIT roundup: Jericho to explore patient control over shared records

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Med-Tech Notes

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People in the News

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MDD's Neurology Extra

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