Event : Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials http://www.rsc.org/events/detail/7048/Regulatory%20Perspectives%20of%20Clinical%20Project%20Management%3a%20Meeting%20FDA%20Requirements%20for%20Clinical%20Trials This is a feed for event : Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials Thu, 11 Sep 2014 13:13:13 +0100 7048 7048 http://www.rsc.org/events/detail/7048/Regulatory%20Perspectives%20of%20Clinical%20Project%20Management%3a%20Meeting%20FDA%20Requirements%20for%20Clinical%20Trials Regulatory Perspectives of Clinical Project Management: Meeting FDA Requirements for Clinical Trials Event dates: 28 February 2012<br/>Event summary: This 90-minute webinar will provide an overview of regulatory management for clinical trials. It will discuss key regulatory aspects of a clinical project such as clinical protocol management, IRB m<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