UK MedTech: Dual Mandate – Patient Safety & Data Privacy After the 2025 PMS Regulations cover art

UK MedTech: Dual Mandate – Patient Safety & Data Privacy After the 2025 PMS Regulations

UK MedTech: Dual Mandate – Patient Safety & Data Privacy After the 2025 PMS Regulations

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 The regulatory landscape for medical devices in Great Britain has just been fundamentally reshaped. Effective June 16, 2025, the Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024 introduce a mandate for manufacturers to intensify their monitoring efforts once devices are on the market. The goal is clear: faster detection of safety issues and better containment of risk.
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In the spirit of reconciliation, Audible acknowledges the Traditional Custodians of country throughout Australia and their connections to land, sea and community. We pay our respect to their elders past and present and extend that respect to all Aboriginal and Torres Strait Islander peoples today.