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    Fundamentals of EU MDR and IVDR – Level 1

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    Website https://www.complianceonline.com/fundamentals-of-eu-mdr-and-ivdr-seminar-training-80624SEM-prdsm?cha | Want to Edit it Edit Freely

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    Deadline: June 14, 2021 | Date: June 24, 2021-June 25, 2021

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

    Updated: 2021-05-18 11:47:16 (GMT+9)

    Call For Papers - CFP

    This 2 day seminar will go into the specifics of the European Union Medical Device Regulation (EU MDR) and the In Vitro Diagnostic Device Regulation (IVDR), provide case studies and share lessons learned so your organization can benefit from the mistakes of others.

    We will review the latest changes to the regulations effective and in force for 2020 and will draw out key developments and key dates with particular emphasis on requirements for US firms shipping materials, parts, and products 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.