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Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
The Adverse Weather and Health Plan (AWHP) aims to protect individuals and communities from the health effects of adverse weather and to build community resilience.
Advises on how planning can manage potential noise impacts in new development.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
This Adverse Weather and Health Plan (AWHP) equity review and impact assessment reviews existing evidence of the risks posed by adverse weather to different populations. It outlines next steps to improve understanding of these risks.
Urgent and clinically significant safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Application form ADV1: registration of a person in adverse possession.
Form ST1: Statement of truth in support of an application for registration based upon adverse possession.
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