Post-Market Surveillance for Medical Devices: Industry Feedback Roundtable

Join techUK for a roundtable discussion on the recently published Post-Market Surveillance (PMS) guidance for medical devices. Released on January 15th, 2025, these regulations strengthen safety monitoring of medical devices in the UK. Industry representatives will have the opportunity to provide direct feedback on the implementation and impact of these new requirements.

The session will focus on how enhanced PMS measures enable swift regulatory action and support the broader healthcare system in protecting patient safety.