4th Workshop – MDR compliance
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Swiss Medtech is organizing a fourth workshop on MDR compliance on 22 May 2019.
- Decision-makers for clinical, vigilance and market surveillance matters
- Development, quality and regulatory managers
- 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
The event’s official language is French.