Event : Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada http://www.rsc.org/events/detail/7091/Medical%20Device%20Adverse%20Event%20Reporting%20and%20Vigilance%20System%20During%20Clinical%20Trials%20and%20Post-Marketing%3a%20US%2c%20EU%2c%20and%20Canada This is a feed for event : Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada Thu, 11 Sep 2014 13:13:13 +0100 7091 7091 http://www.rsc.org/events/detail/7091/Medical%20Device%20Adverse%20Event%20Reporting%20and%20Vigilance%20System%20During%20Clinical%20Trials%20and%20Post-Marketing%3a%20US%2c%20EU%2c%20and%20Canada Medical Device Adverse Event Reporting and Vigilance System During Clinical Trials and Post-Marketing: US, EU, and Canada Event dates: 6 March 2012<br/>Event summary: 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 <br/>Event Venue: Online Event, Palo Alto, 94303, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00