M
Member
Speaking in the House of Lords on 28 November 2024
Debate
Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024Contribution
The instrument will set out in greater detail what must be included as part of a PMS system and a PMS plan. Manufacturers will need to ensure that this includes analysis of relevant data throughout the device’s lifetime, providing a more accurate assessment of device performance and leading to the faster identification and resolution of safety issues.
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