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      The New EU Medical Device Regulation (2017-745) - Mandatory 26-May-2020 in Middletown


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      September 20, 2020

      Sunday   1:00 PM - 2:00 PM

      Compliance Key,364 E Main Street, Suite 1009
      Middletown, Delaware 19709

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      EVENT DETAILS
      The New EU Medical Device Regulation (2017-745) - Mandatory 26-May-2020

      Topic : The New EU Medical Device Regulation (2017-745) - Mandatory 26-May-2020

      Register :https://www.compliancekey.us/webinarDetails?industryId=3&webinarid=1614&speakerid=269&SOURCE=EF_RD

      Discount Coupon : Use this Coupon (NEW2COMPLIANCE) and get (10% Off) On New Signup

      Overview

      This webinar will discuss main differences between current EU Medical Device Directive (MDD) 93/42/EEC and new EU Medical Device Regulation (MDR) 2017-745 and how to ensure compliance with the new MDR requirements that will be mandatory starting 26-May-2020.

      Areas Covered in the Session :

      Device classification
      Conformity routes
      General Safety and Performance Requirements (GSPRs)
      Technical documentation
      Post market surveillance (PMS)
      Clinical evaluation
      UDI
      EUDAMED
      Economic operators

      Speaker Profile :

      Juan M. Campos is a keynote Speaker at Compliance Key. Juan M. Campos is a Medical Device professional with 32+ years of continued industry experience.His main areas of expertise include Quality Assurance, Regulatory Compliance and RegulatoryAffairs. He has led culturally and geographically diverse QA/RA teams in Spain, UK, France,Switzerland, Netherlands, Germany, Portugal, Italy, Greece and Turkey directly reporting to him.

      Contact Info :

      Compliancekey
      https://www.compliancekey.us
      Email : support@compliancekey.us
      Phone : +1 717-208-8666

      Categories: Business & Networking

      Event details may change at any time, always check with the event organizer when planning to attend this event or purchase tickets.

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