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Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada

6 March 2012, Palo Alto, United States


Introduction
This 3-hr virtual seminar will discuss the requirements and compliance in medical device adverse event reporting and medical device surveillance/vigilance system in the US, Europe and Canada. It is designed to help the audience with their global compliance in adverse event reporting and surveillance/vigilance system during pre- and post-marketing.
Venue
Online Event

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

Organised by
ComplianceOnline
Contact information
ComplianceOnline
2600 E. Bayshore Road, Palo Alto, 94303, United States of America
+1-650-620-3915
Contact us by email

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