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