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How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
Sections (2.01 - 2.41) last updated January 2024.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
How to create a model of how your digital health product works and choose measures for your evaluation.
Guidance for manufacturers, importers and distributors on the Product Security and Telecommunications Infrastructure Act 2022 and Regulations 2023.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Millions invested in eight innovative companies behind lifesaving new medical technology which could destroy liver cancer tumours, detect Alzheimer’s and quickly spot those at risk of stroke
Evaluations made by the Rapid Review Panel (RRP) on submitted products.
The UK’s consumer connectable product security regime came into effect on 29 April 2024. Businesses in the supply chains of these products now need to be compliant with the legislation.
The Rapid Review Panel (RRP) assesses innovative infection prevention and control products, equipment and materials for potential use in the NHS.
Product Recall for 5 in 1 Heat Press Machine presenting a serious risk of electric shock.
Product Safety Report for Multipurpose Ladder presenting a serious risk of injuries.
Overview of UK research infrastructure to develop new medical technology and advantages of investment in the UK's life science sector to support new products.
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