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/16451/Webinar%20On%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 Mon, 06 Oct 2014 12:18:54 +0100 16451 16451 http://www.rsc.org/events/detail/16451/Webinar%20On%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: 22 October 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.<br/>Event Venue: Compliance Trainings, Mississauga, L5V 2V5, Canada Mon, 06 Oct 2014 12:18:54 +0100 2014-10-06T12:18:54+01:00