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Draft Guidance for Device Industry and FDA - Postmarket Surveillance - Webinar By GlobalCompliancePanel

25 October 2011, Wilmington, United States


Introduction
This webinar will provide an overview and guidance to firms that are either going through or preparing to go postmarket surveillance activities.

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Venue
online training webinar

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

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Organised by
globalcompliancepanel

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