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
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By Compliance2go
4 October 2011, Houston, United States
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Compliance2go Webinar
Online, Compliance2go Webinar, 10777 Westheimer Suite 1100, Houston, Texas, Houston, 77043, United States
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