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Meet the U.S. FDA's Tougher Requirements for the 510(k) - Webinar By GlobalCompliancePanel

20 March 2013, Fremont, United States


Introduction
This webinar will evaluate medical device review routes under Exempt, 510(k) / PMN, and PMA, as both a process and as documentation / submissions. The 510(k) process and submission documentation, the role of the IDE, and the PMA process and submission documentation will be evaluated and discussed.

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Venue
Online Training

Livermore Common, Online Training, California, Fremont, 94539, United States

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Organised by
GlobalCompliancePanel
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