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Qarad webinar: MDR compliance

30.03.2023
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Everything you need to know about the MDR compliance

 

Qarad organises a free webinar on 30 March 2023 to help Swiss Medical Device manufacturer feeling a bit lost when it comes to MDR compliance.

 

Qarad’s Regulatory Affairs Expert, Anne-Sophie Grell, will help you navigate the winding road to MDR compliance. The following topics will be covered:

  • Types of medical devices and classification
  • Requirements: QMS, ISO 13485, technical documentation, Unique Device Identification (UDI)…
  • Different economic actors like Notified bodies and Eudamed

 

🗓️ When: Thursday, 30 March 2023, 3 pm

▶️ Registration: here