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2020 - Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation

Date2020-10-27 - 2020-10-28

Deadline2020-10-17

VenueVirtual Seminar, USA - United States USA - United States

KeywordsEU MDR 745/2017; EN ISO 13485:2016; Iso 13485 2016 standard

Websitehttps://www.complianceonline.com/en-iso-...

Topics/Call fo Papers

The new scope of the EU MDR 2017/745
The obligations and roles of the EU MDR 2017/745
How work the regulation and the EN ISO 13485:2016 together?
New and updated processes required by the EU MDR 2017/745
How to implement the required changes until May 2021?

Other CFPs

  1. Fundamentals of EU MDR and IVDR – Level 1
  2. Laboratory Inspection and Auditing
  3. Statistics for Quality Control
  4. The Drug Development Process from Concept to Market
  5. Project Management for Human Resources

Last modified: 2020-09-26 23:28:21