Event : Master Verification & Validation Planning under U.S. FDA CGMP, ICH Q-series and ISO 13485-14971 Requirements - Webinar By GlobalCompliancePanel http://www.rsc.org/events/detail/7191/Master%20Verification%20%26%20Validation%20Planning%20under%20U.S.%20FDA%20CGMP%2c%20ICH%20Q-series%20and%20ISO%2013485-14971%20Requirements%20-%20Webinar%20By%20GlobalCompliancePanel This is a feed for event : Master Verification & Validation Planning under U.S. FDA CGMP, ICH Q-series and ISO 13485-14971 Requirements - Webinar By GlobalCompliancePanel Thu, 11 Sep 2014 13:13:13 +0100 7191 7191 http://www.rsc.org/events/detail/7191/Master%20Verification%20%26%20Validation%20Planning%20under%20U.S.%20FDA%20CGMP%2c%20ICH%20Q-series%20and%20ISO%2013485-14971%20Requirements%20-%20Webinar%20By%20GlobalCompliancePanel Master Verification & Validation Planning under U.S. FDA CGMP, ICH Q-series and ISO 13485-14971 Requirements - Webinar By GlobalCompliancePanel Event dates: 21 March 2012<br/>Event summary: FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in many companies.<br/>Event Venue: Online Training, Wilmington, 19801, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00