Medical Devices: EU Directives, CE marking, ISO Certification and the NEW Device Regulations coming to the EU
Website https://www.complianceonline.com/medical-devices-eu-directives-guidance-documents-ce-marking-process |
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Deadline: November 28, 2020 | Date: December 08, 2020
Venue/Country: U.S.A
Updated: 2020-11-29 03:18:33 (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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