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EU MDR: One More Year On The Clock. Use It Wisely...

Benchmark Your Medical Device Regulatory Strategy With Competent Authority Feedback, Notified Body Guidance And Leading Industry Case Studies

Navigate EU MDR Timelines, The Medical Device Selection Process, EUDAMED And More...

Implementing The EU Medical Device Regulation: 2020 Highlights


Lessons Learnt So Far
Lessons Learnt So Far
  • Hear from leading manufactures Cochlear, Medtronic, Straumann and Zimmer Biomet on strategies for being MDR compliant
  • Get access to Notified Bodies in a pain points panel with NSAI and TÜV SÜD
  • Seeking advice on implementing a UDI system? Zimmer Biomet share practical advice...
What’s Next?
What’s Next?
  • Get to grips with the impact of COVID-19 on the EU MDR with Axon Lawyers LLP
  • With an extra 2 years on the clock, hear from Richard Houlihan on how to prepare for EUDAMED
  • Gain clarification on National Requirements from the MHRA 
Elsewhere At The MedTech Summit...
Elsewhere At The MedTech Summit...

Take a look at the 8 other MedTech Summit conference tracks to see what else is on the agenda for you:

  • Navigate CER requirements and "sufficient" clinical evidence under the EU MDR in the Clinical Evaluations & Investigations track
  • Find out how the first experiences of Manufacturer's Incident Reporting is going in the Post Market Surveillance & Vigilance track   
  • Join the Software and AI track for advice and insights on the unique challenges for software under the EU MDR
  • Examine the movement toward EU MDR compliance for commercial combination products in the pharma industry in the Drug Device Combination Products track
See The Full MedTech Summit Agenda