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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
The information clients, principal designers, principal contractors and accountable persons need to keep.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Weekly UKHSA report for the 2025/26 season, monitoring respiratory viruses.
A digital platform designed to facilitate the reporting, monitoring, and management of medical device incidents.
Reports presented to Parliament pursuant to Section 17 of the Public Libraries and Museums Act 1964
A collection of investigatory reports published by the National Measurement and Regulation Office Enforcement Services.
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How to apply for a full or partial completion certificate after building work on a higher-risk building has been completed.
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