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    11.03.19
    ECM white paper: PLANNING FOR IMPLEMENTATION OF THE EU MDR New ECM White Paper! PLANNING FOR IMPLEMENTATION OF THE EU MDR - Are you prepared?

    Learn how to better prepare for the new requirements of the EU Medical Device Regulation (MDR).

    Topics included:
    - Provisions of the new MDR
    - Notified Bodies and the Transition Process
    - Clinical Evidence Expectations in the New MDR
    - Post-Market Surveillance (PMS)
    - What is the Unique Device Identification (UDI)
    - What is an Implant Card
    - External Vigilance
    - Summarizing an Implementation Strategy

    Fill the form to request it https://lnkd.in/g4UkHMZ 
    Or contact our Sales Manager Antonio Balassone to have it and make your questions antonio@entecerma.it 

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