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There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
We’re working to help people securely prove who they are without having to rely on physical documents.
Guiding principles for the use of Predetermined Change Control Plans (PCCPs) for managing rapid product changes.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Advice on writing clear notices and maximising replies to your FSNs.
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (9 May 2024) launched AI Airlock, its new regulatory sandbox for AI as a Medical Device (AIaMD).
How test manufacturers or distributors can apply for approval of their tests to sell on the UK market.
Government outlines action to make UK a world leader in tackling ethnic and other biases in medical devices.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
Detention services order 05/2014 about the installation and removal of electronic monitoring devices from detainees.
Using smart meters to automate charging of electric vehicles.
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
How the supply of medical devices from Great Britain into Northern Ireland works.
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