Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Program

Event Name:	Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Program
Description:	This Medical device training will be discussing 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 commercializing products. 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 on commercializing products. The course covers all relevant topics in brief associated with the Directives and Guidance Documents, the reasons behind their introduction and a review of methods for effective implementation.
Type of Event:	Education - Training Events
Event Agenda:
Event Location:	Online Event
Event City:	Palo Alto
Type of Venue:	Outdoors - No Venue
Station/Stop:
Directions:
Event Start Date	05-Apr-12