Event : FDA's Revised [Draft] Guidance on Medical Device Changes and the 510(k) - Webinar By GlobalCompliancePanel http://www.rsc.org/events/detail/6884/FDA's%20Revised%20[Draft]%20Guidance%20on%20Medical%20Device%20Changes%20and%20the%20510(k)%20-%20Webinar%20By%20GlobalCompliancePanel This is a feed for event : FDA's Revised [Draft] Guidance on Medical Device Changes and the 510(k) - Webinar By GlobalCompliancePanel Thu, 11 Sep 2014 13:13:13 +0100 6884 6884 http://www.rsc.org/events/detail/6884/FDA's%20Revised%20[Draft]%20Guidance%20on%20Medical%20Device%20Changes%20and%20the%20510(k)%20-%20Webinar%20By%20GlobalCompliancePanel FDA's Revised [Draft] Guidance on Medical Device Changes and the 510(k) - Webinar By GlobalCompliancePanel Event dates: 25 January 2012<br/>Event summary: This webinar will discuss the new draft guidance document from the FDA: "510(k) Device Modifications: Deciding When to Submit a 510(k) for a Change to an Existing Device", dated July 27, 2011.<br/>Event Venue: Online Training, Wilmington, 19801, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00