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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

July 16, 2012

View Archived Issues

Washington roundup: 510(k)s included in overhaul of the 1999 pre-sub guidance

FDA has published a draft overhaul of the 1999 document dealing with pre-IDE submissions, substantially expanding the scope of the program to include devices co-regulated by the Center for Biologics Evaluation and Research, but FDA is also offering pre-submission interaction for 510(k) applications as well. Read More

K2M expands biologics line via LifeNet partnership

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International report: Varian in partnership to offer its RapidArc treatment in Venezuela

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The IPO problem keeps tick, tick, ticking for small med-techs

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Deals roundup: Synergy completes offer for shares of SRI/Surgical Express

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Financings roundup: TearLab to raise about $7.9M in registered share offering

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HIT roundup: Vocera Communications System achieves JITC certification

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Med-Tech Notes: Lab21 offers companion diagnostic in the U.S.

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Agreements roundup: Derma Sciences gets Nimbus technology from Quick-Med

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People in the News

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Product Briefs

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MDD's Neurology Extra

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