Event : Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971 Requirements - Webinar By GlobalCompliancePanel http://www.rsc.org/events/detail/5683/Developing%20the%20Master%20V%26V%20Plan%20to%20Meet%20U.S.%20FDA%2c%20ISO%2013485%20and%2014971%20Requirements%20-%20Webinar%20By%20GlobalCompliancePanel This is a feed for event : Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971 Requirements - Webinar By GlobalCompliancePanel Thu, 11 Sep 2014 13:13:13 +0100 5683 5683 http://www.rsc.org/events/detail/5683/Developing%20the%20Master%20V%26V%20Plan%20to%20Meet%20U.S.%20FDA%2c%20ISO%2013485%20and%2014971%20Requirements%20-%20Webinar%20By%20GlobalCompliancePanel Developing the Master V&V Plan to Meet U.S. FDA, ISO 13485 and 14971 Requirements - Webinar By GlobalCompliancePanel Event dates: 11 May 2011<br/>Event summary: Overview: FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in many companies. One major failing is lack of sufficient or targeted risk-based company-wide V&V plan<br/>Event Venue: Online Training Webinar, Wilmington, 19801, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00