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    Post Market Surveillance with the new Medical Device Regulation EU MDR 745/2017

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    Website https://www.complianceonline.com/post-market-surveillance-eu-mdr-745-2017-webinar-training-706121-pr | Want to Edit it Edit Freely

    Category

    Deadline: September 20, 2019 | Date: September 20, 2019

    Venue/Country: U.S.A

    Updated: 2019-08-22 19:20:50 (GMT+9)

    Call For Papers - CFP

    This webinar will help you understand the requirements of the new medical device regulation EU MDR 745/2017 and teach you how to create the reports. The understanding of the changes and how to implement last-minute changes until May 2020 is essential to keep your certificates and to sell your products after May 2020 to the European Union.

    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.