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    EU ISO 13485:2016 Medical Device Quality Management System

    View: 260

    Website https://www.complianceonline.com/iso-13485-2016-medical-device-quality-management-system-webinar-tra | Want to Edit it Edit Freely

    Category

    Deadline: October 02, 2019 | Date: October 02, 2019

    Venue/Country: U.S.A

    Updated: 2019-07-04 21:23:49 (GMT+9)

    Call For Papers - CFP

    What are EU Notified-Body expectations under ISO 13485 and the MDR – with the recent major revisions to both?

    How can a company develop and maintain a dual QMS.

    Basic Systems / SOPs.

    Brief discussion of ISO 14971 (Device Risk Management) and IEC 62366-1 (Use Engineering / Human Factors) and where they fit.

    Current areas of EU concern.

    Maintaining compliance under increasing regulatory expectations.

    Similarities and differences in the FDA and EU QMS’.


    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.