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The 510(k) Process and Risk Management - Webinar By GlobalCompliancePanel

8 September 2011, Wilmington, United States


Introduction
This webinar will discuss FDA concerns in medical device safety expressed in reports on 510(k) products.

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Venue
online training webinar

online training webinar, 1000 N West Street, Suite 1200, Wilmington, 19801, United States

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Organised by
globalcompliancepanel
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