At the 12thMedical Devices Symposium you will learn:
- All about new MDR transition periods and how you can benefit from them
- The positions from European Commission, industry and Notified Bodies
- The impact of EU requirements on sustainability, ESG and (robust) supply chains
- The importance of the European Health Data Space (EHDS)
- The outlook to non-EU-regulatory systems for medical devices (such as US FDA)
Register now!