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Evaluation ViewAttendees 44

Devices (includes Medical Devices and In Vitro Diagnostics)

UKCA & Market Developments

Wednesday, September 18, 2024
2:15 PM – 3:15 PM PDT
Location/Room: 104 C
Explanation of the current UKMDR 2002 for medical devices and IVDs including implementation of PMS requirements. Introduction to the proposed Core and Enhanced UKMDR including proposed timings and transitions. Panel discussion with perspectives from Industry, UK Approved Bodies, UK Competent Authority, UK Rep followed by Q+A

Learning Objectives:

  • Understand the current status of the UKMDR and transitional arrangements
  • Understand the latest developments of the UK MDR including the Core and Enhanced regulation including the proposed implementation
  • Understand the perspective of all stakeholders including Industry, UK Approved Bodies, UK Competent Authority, UK Rep