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Have your got your EU MDR PMS & Vigilance strategy in place? 1 more year. 1 more chance.

Regulatory Insights On PSURs. Create Robust PMS Plans. Updates On Manufacturer's Incident Reports

Overcome The Obstacles With Notified Body Advice And Practical Industry Examples

2020 Highlights: Post Market Surveillance & Vigilance


All You Need To Know
All You Need To Know
  • Join Notified Bodies NSAI, IMQ and TÜV SÜD to discuss their requirements for Post Market Surveillance
  • Novartis were the first company to get a CE mark for their Concept1 inhaler under the EU MDR. Hear about their first 9 months of PMS.
  • Want to EU MDR proof your PMS plan? Gain leading insights from Abbott
  • Get up to date perspectives on Periodic Safety Update Reports (PSURs) with feedback from Abbott 
Post Market Reporting
Post Market Reporting
  • Hear the latest on how the first experiences of Manufacturer Incident Reporting (MIR) have gone with Johnson and Johnson
  • Telefex provide practical insights on Serious Incident Reporting 
  • Update your strategies to ensure your risk management and complaint system is MDR ready with NSF and Resmed
  • Benefit from a joint session with the Clinical Evaluations & Investigations audience: Learn how to handle Post Market Clinical Follow-up (PMCF)
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:

  • Shine a light on US Post Market Safety Reporting requirements for combination products in our Drug Device Combination Products track
  • Be Prepared for China's increased focus on Post Market Surveillance with speakers from NMPA in the Medical Device Regulatory Affairs in Global Markets track
  • Join our EU Medical Device Regulation track to get updates, hear first-hand experiences and benchmark EU MDR implementation with your peers
See The Full MedTech Summit Agenda