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Guidance to help you plan and prepare for implementing artificial intelligence (AI).
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Explainer for the pharmaceutical industry on the implementation of Pharmacovigilance requirements during the transition time from the date the revised VMR have effect in GB to 17 May 2027.
Guidance for local authorities and operators of local bus services in England.
Guidance on the updates to reporting forms following implementation of the Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024.
The RPC and Better Regulation Executive (BRE) have compiled a collection of links that may be useful for departments to use when writing impact assessments.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Details how the Prime Minister's challenge on dementia 2020 will be met.
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