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How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to apply for a clinical trial from 28 April 2026, including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Provides detailed information on both potential types of information and evidence, and the correct way to process and record such information.
Training material and guidance on how to use and implement the International Protocol on the documentation and investigation of sexual violence in conflict.
Sets out issues to consider when collecting testimonies or statements from survivors or witnesses.
The review of the safety of isotretinoin has concluded.
Experts on comparative international healthcare provision are invited to submit expressions of interest by the close of 22 August 2025.
Sets out key practical issues to consider when planning investigation or documentation.
RAIB investigation reports, safety digests, and urgent safety advice by year of publication.
Potential reviewers of country of origin information are invited to submit expressions of interest by the close of 22 August 2025.
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