Live Seminar On Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By Compliance2go

5 December 2013, Houston, United States

Introduction

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