Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs - Medical Device Webinar By ComplianceOnline | Thursday, December 16th, 2010 | Palo alto, United States

Contact Person : Admin; Last Date for the submission of abstract : Not Available ; Description : This Medical device training will be discussing 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.

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Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs - Medical Device Webinar By ComplianceOnline

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