Driving ‘A safer healthcare ecosystem’

The European Union Medical Device Regulation (EU MDR) brings a wider and clearer regulatory scope which enforces stricter requirements on manufacturers and notified bodies. 

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  • The important dates of application
  • How the MDR will affect medical device R&D and market access
  • How the MDR will impact current and future CE marks
  • Why clinical evidence and data is of utmost importance

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