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EN ISO 5: 2023 - Lead Auditor EN ISO 13485:2021 and EU MDR 2017/745 - Regulation
Website https://www.complianceonline.com/80654SEM-prdsm?channel=ourglocal |
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Category ISO 13485, EU MDR 2017
Deadline: January 26, 2023 | Date: January 27, 2023
Venue/Country: Virtual Seminar, U.S.A
Updated: 2023-01-10 00:54:34 (GMT+9)
Call For Papers - CFP
The medical device regulation EU MDR 745/2017 in the European Union has a lot of requirements. This regulation is also stronger connected to the EN ISO 13485:2021. The first key for the understanding and the implementation of the changes is the knowledge about the relationship between the EN ISO 13485:2021 and the EU MDR 2017/745. The second key is to understand, which parts of the EU MDR 2017/745 are not covered by the EN ISO 13485:2021. These not covered paragraphs and requirements must be additional implemented into the quality management system.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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