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🗓️ Date: 8 May 2025
⏰ 4:00 – 5:00 PM CET | 3:00 – 4:00 PM GMT
đź”— Register Now and Save Your Spot!

 

The latest UK Post-Market Surveillance Regulations will have significant implications for your business. Join our webinar to explore the purpose of the new regulations, the key changes, and the differences and impact on CE-marked medical devices in the UK.

 

Learning objectives

  • Learn about the new UK PMS requirements
  • Learn about the impact of the new regulations on your post-market procedures, vigilance procedures and your CE-marked medical devices in the UK

Speakers

  • Dennis Sarwin, Team manager Global Registrations & Consultant
  • Melissa Smits, Projectmanager & Senior Global Registrations Specialist

Don’t miss this opportunity to gain actionable insights and stay ahead on UK regulations!

 

Register Now >>
Ben Kemp