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Upper Tribunal Administrative Appeals Chamber decision by Judge Johnson on 7 January 2025
Upper Tribunal Administrative Appeals Chamber decision by Judge Johnston on 30 December 2024
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Blogs where government organisations talk about their work and share information and ideas.
Submissions related to human medicines need to be submitted directly to the MHRA.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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