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.
Live webinar on Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs By compliance2go
4 June 2012, Houston, Texas, United States
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Online, 10777 Westheimer Suite 1100, Houston, Texas, 77042, United States
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