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Draft Guidance for Device Industry and FDA - Postmarket Surveillance

8 December 2011, Palo Alto, United States


Introduction
This webinar will cover FDA's Draft Guidance on Post market Surveillance Studies for device manufacturers Under Section 522. It will help you understand the proposed changes and agency expectations regarding different stages of Post market Surveillance Studies.

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Venue
Online Event

Online Event, 2600 E. Bayshore Road, California, Palo Alto, 94303, United States

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ComplianceOnline
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