Event : LIve Webinar- Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs http://www.rsc.org/events/detail/11384/LIve%20Webinar-%20Medical%20Devices%3a%20EU%20Directives%2c%20Guidance%20Documents%2c%20CE%20Marking%20Process%20and%20ISO%20Certification%20Programs This is a feed for event : LIve Webinar- Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs Thu, 11 Sep 2014 13:13:13 +0100 11384 11384 http://www.rsc.org/events/detail/11384/LIve%20Webinar-%20Medical%20Devices%3a%20EU%20Directives%2c%20Guidance%20Documents%2c%20CE%20Marking%20Process%20and%20ISO%20Certification%20Programs LIve Webinar- Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs Event dates: 17 July 2014<br/>Event summary: This webinar is focused on understanding the requirements of the Medical Device Directives, their linkage to the EU Clinical Trial Directive and the requirements of CE Marking and ISO Certification <br/>Event Venue: Online, Houston, 77042, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00