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Post Market Surveillance & Vigilance

We're PMS and Vigilance Ready. Are you?

2018 Highlights Include:

Overcome your PMS & vigilance obstacles
  • How are different companies practically implementing new requirements?
  • Immerse yourself in PMS plan compilation
  • Timelines for post market reporting are changing: Can you keep up?
  • Ensure a best practice approach for Field Safety Corrective Action (FSCA) reporting
  • Leverage your PMS data to become better informed about your products
Competent Authority, Notified Body and industry perspectives from:
  • National Institute for Public Health and the Environment (RIVM)
  • TÜV SÜD Product Service
  • Cendres + Métaux SA
  • Medtronic
  • Terumo Europe N.V.
Sharing experiences and strategies

We’ll be hosting interactive panel discussions on:

  • How are different companies implementing new PMS and vigilance requirements?
  • How can I be compliant with the EU MDR post market activities and reports?

Free On-Demand Content

Webinars. Webinars. Webinars.

EU MDR Labeling Compliance: Learn the Lessons from UDI

Speakers:
Mark Cusworth, VP Research and Development, PRISYM ID
Andrew Love, VP Capability Development, Be4ward
WATCH THIS WEBINAR


Latest status and practical experience of implementing the new EU MDR

Speaker:
Bassil Akra, Vice President, Global Focus Teams (Cardiovascular, Orthopeadic and Clinical), TÜV SÜD Product Service GmbH, Germany
WATCH THIS WEBINAR