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    Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation

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    Website https://www.complianceonline.com/en-iso-13485-2016-eu-mdr-2017-745-seminar-training-80654SEM-prdsm?c | Edit Freely

    Category

    Deadline: October 17, 2020 | Date: October 27, 2020-October 28, 2020

    Venue/Country: Virtual Seminar, U.S.A

    Updated: 2020-09-26 22:34:58 (GMT+9)

    Call For Papers - CFP

    The new medical device regulation EU MDR 745/2017 in the European Union has a lot of new requirements. This new upcoming regulation is also stronger connected to the EN ISO 13485:2016. The understanding of this changes and how to implement last minute changes until May 2021 is essential to keep your certificates. The first key for the understanding and the implementation of the changes is the knowledge about the interfaces between the EN ISO 13485:2016 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 13485:2016. These not covered paragraphs and requirements must be additional implemented into the quality management system until May 2020. The time is short and immediately action is required.

    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.