Event : Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By Compliance2go http://www.rsc.org/events/detail/6284/Medical%20Devices%3a%20EU%20Directives%2c%20Guidance%20Documents%2c%20CE%20Marking%20Process%20and%20ISO%20Certification%20Programs%20By%20Compliance2go This is a feed for event : Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By Compliance2go Thu, 11 Sep 2014 13:13:13 +0100 6284 6284 http://www.rsc.org/events/detail/6284/Medical%20Devices%3a%20EU%20Directives%2c%20Guidance%20Documents%2c%20CE%20Marking%20Process%20and%20ISO%20Certification%20Programs%20By%20Compliance2go Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By Compliance2go Event dates: 4 October 2011<br/>Event summary: 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 on commercializi<br/>Event Venue: Compliance2go Webinar, Houston, 77043, United States Thu, 11 Sep 2014 13:13:13 +0100 2014-09-11T13:13:13+01:00