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How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
The Planning Inspectorate appeals casework portal - Terms and Conditions
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
The review of the safety of isotretinoin has concluded.
The Planning Inspectorate appeals casework portal - Troubleshooting
Advice on how to stay secure online from the UK's National Cyber Security Centre.
British travellers to the US must register with the Electronic System for Travel Authorisation (ESTA) before their journey
Submissions related to human medicines need to be submitted directly to the MHRA.
As a member of the public, owner or occupier of coastal access land, find out how you can comment or object on new access proposals.
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