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