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18 - 22 October 2021
Virtual EventDelivered in CEST time zone

Post Market Surveillance: Sink or Swim?

Ride the wave to sustainable long-term EU MDR compliance with expert guidance from Competent Authority, Notified Body and industry pioneers

Including focused insights for risk management, state of the art, PSUR, PMCF, SaMD and more!

Take Your PMS Strategy To World Class Levels With Expert Guidance

PMS: Real World Experiences And Advice

  • Experience with building and maintaining a robust Post Market Surveillance Plan
  • Creating an MDR PMS plan for your MDD products
  • Navigate surveillance for Software as a Medical Device

Understand The Regulatory Requirements

  • Explore Benefit vs Risk through leading case studies and panel discussion
  • Dive into the details of Post Market Clinical Follow-up compliance with Cook, Merit Medical and Sirtex
  • Get best practice advice for creating a compliant Periodic Safety Update Report (PSUR)

Streamline Post Market Surveillance Processes With

  • Competent Authority guidance with FAMPH
  • Panel Discussion: Notified Body feedback from GMED and IMQ
  • Gain industry advice for data-driven QMS alignment with COOK Medical