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    EU Medical Device Regulation (MDR) – Updated CE Marking Process and ISO 13485:2016 Expectations

    View: 134

    Website https://www.complianceonline.com/eu-medical-device-regulation-ce-marking-process-and-iso-13485-2016- | Want to Edit it Edit Freely

    Category

    Deadline: February 19, 2019 | Date: February 19, 2019

    Venue/Country: U.S.A

    Updated: 2019-01-17 19:47:54 (GMT+9)

    Call For Papers - CFP

    This EU Medical Device Regulation (MDR) 90-minute webinar will discuss the recently developed regulation and its impact on the future compliance and registration of medical devices in the EU. It includes specific insights from direct involvement and work within the EU and the Commission's major improvement objectives to their system today. Areas of change between the prior Medical Device Directive (MDD) and the MDR will be discussed as well as expectations for how to implement ISO-13485:2016.

    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.