Event : Webinar On - Master Validation Planning To Meet U.S. FDA cGMP, ISO 13485, and ICH Q9 / ISO 14971 Requirements http://www.rsc.org/events/detail/10468/Webinar%20On%20-%20Master%20Validation%20Planning%20To%20Meet%20U.S.%20FDA%20cGMP%2c%20ISO%2013485%2c%20and%20ICH%20Q9%20/%20ISO%2014971%20Requirements This is a feed for event : Webinar On - Master Validation Planning To Meet U.S. FDA cGMP, ISO 13485, and ICH Q9 / ISO 14971 Requirements Thu, 11 Sep 2014 13:13:13 +0100 10468 10468 http://www.rsc.org/events/detail/10468/Webinar%20On%20-%20Master%20Validation%20Planning%20To%20Meet%20U.S.%20FDA%20cGMP%2c%20ISO%2013485%2c%20and%20ICH%20Q9%20/%20ISO%2014971%20Requirements Webinar On - Master Validation Planning To Meet U.S. FDA cGMP, ISO 13485, and ICH Q9 / ISO 14971 Requirements Event dates: 5 March 2014<br/>Event summary: This 90 minute in-depth webinar discusses the FDA Warning Letters and recent high-profile recalls indicate major cGMP deficiencies in big name device and pharma companies, many going back to insuffi<br/>Event Venue: Online, Mississauga, L5V 2V5, Canada Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00