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4th Workshop – MDR compliance

14.05.2019
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Swiss Medtech is organizing a fourth workshop on MDR compliance on 22 May 2019.

 

TARGET AUDIENCE

  • Manufacturers
  • Representatives
  • Decision-makers for clinical, vigilance and market surveillance matters
  • Development, quality and regulatory managers

 

AGENDA

  • Impact of MDR on CE marking for OEM/OBL products
  • Introduction to the UDI in Europe and comparison with EU/US
  • System quality and differences between ISO 13485:2016 /MDD and the MDR

 

PROGRAMME AND REGISTRATION

https://www.frn.swiss-medtech.ch/sit

The event’s official language is French.