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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.
Venue
Online Training

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

Organised by
GlobalCompliancePanel
Contact information
Mr John Robinson
Livermore Common, Fremont, 94539, United States of America
8004479407
Contact us by email

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