Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs
Website https://www.complianceonline.com/medical-devices-eu-directives-guidance-documents-ce-marking-process |
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Deadline: May 23, 2019 | Date: May 23, 2019
Venue/Country: U.S.A
Updated: 2019-04-10 17:50:31 (GMT+9)
Call For Papers - CFP
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.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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