Skip to main content
RAPS Euro Convergence 2025 Main banner
Icon Legend
This session is not in your schedule.
This session is in your schedule. Click again to remove it.
Presentation Icons
Learning Level: Foundational
Learning Level: Foundational
Learning Level: Intermediate
Learning Level: Intermediate
Learning Level: Advanced
Learning Level: Advanced
Learning Level: Expert
Learning Level: Expert
Networking Event
Networking Event
Sponsor Presentation
Sponsor Presentation
Ticketed Event
Ticketed Event
Evaluation

Medical Devices

UK Regulatory Landscape: UK MDR Amendments and Impact

Thursday, May 15, 2025
10:45 - 11:45 CEST
Location: Studio 211 + 212 (level 2)
Description: The UK MDR is about to go through its biggest update in 20 years and this presentation and panel discussion will provide an overview of the anticipated changes to the regulatory requirements for medical devices and IVDs entering the United Kingdom (UK) market.

This panel will share insights about these evolving UK MDR amendments, including new PMS requirements, and their impact on medical device and IVD manufacturers.

The attendees will gain an understanding of the Approved Body perspective of current and future UK regulatory requirements for medical devices and IVDs which will aid them in navigating their path to compliance.

In addition, this session will provide discussion of other potential routes to the UK market such as IDAP.

Learning Objectives:

  • Understand the anticipated UK MDR amendments and their impact
  • Have awareness of UK specific options for entering the market such as IDAP
  • Understand the UK Approved Body perspective of compliance with UK regulations