This site is part of the Informa Connect Division of Informa PLC

This site is operated by a business or businesses owned by Informa PLC and all copyright resides with them. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Registered in England and Wales. Number 3099067.


EU MDR: The Deadline Is Approaching. Are you Ready?

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

Lessons Learnt So Far
  • Hear from leading manufactures Bausch and Lamb, Medtronic and Cochlear on strategies for being MDR compliant
  • MDCG members give the latest guidance and updates on the MDR implementation
  • Get access to Notified Bodies in a pain points panel with BSI, IMQ, NSAI, SGS and TÜV SÜD 
  • Seeking advice on implementing a UDI system? You're in the right place...
What’s Next?
  • With an extra 2 years on the clock, hear from Richard Houlihan on how to prepare for EUDAMED
  • What's the state of play with the EU MDR post Date of Application?  
  • Gain clarification on National Requirements post EU MDR from DKMA and the MHRA 
  • Which medical devices are at risk in Europe due to the EU MDR? Hear the latest from the NHS
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:

  • Hear the latest on Expert Panels in our Clinical Evaluations & Investigations track: Where are we now?
  • Find out how the first 6 months of Manufacturer's Incident Reporting is going in the Post Market Surveillance & Vigilance track   
  • Join the Software and AI track for classification updates for medical device software under the EU MDR
  • Examine the impact of the EU MDR Article 117 on Drug Delivery Devices in the Drug Device Combination Products track
See The Full MedTech Summit Agenda