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Changes in the EU Medical Device Directives; 2010 Modifications and the 2012 Recast of the MDD Directives - Webinar By GlobalCompliancePanel

13 March 2012, Wilmington, 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.
Venue
Online Training

Online Training, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States

Organised by
GlobalCompliancePanel
Contact information
Mr webinars web
Online Training, 1000 N West Street, Suite 1200, Wilmington, 19801, United States of America
8004479407
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