Event : Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs http://www.rsc.org/events/detail/4766/Clinical%20Trial%20Regulations%20and%20GCP%20Compliance%20as%20they%20relate%20to%20Adverse%20Events%20-%20How%20to%20Assess%20and%20report%20AEs%20and%20SAEs This is a feed for event : Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs Thu, 11 Sep 2014 13:13:13 +0100 4766 4766 http://www.rsc.org/events/detail/4766/Clinical%20Trial%20Regulations%20and%20GCP%20Compliance%20as%20they%20relate%20to%20Adverse%20Events%20-%20How%20to%20Assess%20and%20report%20AEs%20and%20SAEs Clinical Trial Regulations and GCP Compliance as they relate to Adverse Events - How to Assess and report AEs and SAEs Event dates: 19 October 2010<br/>Event summary: This adverse event reporting Webinar/training will discuss the clinical trial regulations requirements with respect to adverse event and explain how to assess and report AEs and SAEs.<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