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.

Master The Legal Implications Of The EU MDR With Expert Advice, Case Studies And Interactive Discussions

Get To Grips With Legislation And Legal Challenges For Medical Device Manufacturers

With Leading Lawyers, Competent Authority And Notified Body Perspectives

2020 Highlights: Navigate The Legal Challenges Of The EU MDR


Expert Legal Advice On Your Top Regulatory Challenges
Expert Legal Advice On Your Top Regulatory Challenges
  • Transitional provisions under the EU MDR: What constitutes a "significant change"?
  • Can you legally challenge decisions of your Notified Body? Find out the current state of play...
  • Claims requirements: Talking labelling, advertising & instruction
Practical Legal Challenges: Solutions And Advice
Practical Legal Challenges: Solutions And Advice
  • Roles, responsibility and liability for the Person for Responsible for Regulator Compliance (PRRC)
  • EU MDR  & new Product Liability Directive: Hear the latest on liability claims
  • Delve into IP & data compliance for digital data and AI
Elsewhere At The MedTech Summit...
Elsewhere At The MedTech Summit...
  • Attend our EU Medical Device Regulation track for comprehensive coverage of the latest regulatory guidance, case studies and lessons learned under the EU MDR
  • Join our EU IVD Regulation and Strategy track to get updates and hear first-hand experiences of EU IVDR implementation
  • Hear the latest regulatory developments from around the world in our Medical Device Regulatory Affairs in Global Markets track
See The Full MedTech Summit Agenda