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    Post-Market Activities in the EU-MDR — A Detailed Analysis

    View: 104

    Website https://worldcomplianceseminars.com/upcoming_webinar | Edit Freely

    Category Quality Assurance, Regulatory Affairs

    Deadline: January 30, 2020 | Date: January 30, 2020

    Venue/Country: Online Webinar, U.S.A

    Updated: 2020-01-04 17:37:43 (GMT+9)

    Call For Papers - CFP

    Recently, the European Union has revised the regulatory requirements governing medical devices; including the establishment of new expectations and approaches to post-market surveillance. Mandatory compliance to the new European Medical Device Regulation (MDR) is set for 26 May 2020.

    Session Highlights:

    Topic 1: Benefits of Post-Market Surveillance

    Topic 2: Review the new EU-MDR 2017/745

    Topic 3: Risk Management

    Speaker:

    Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation


    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.