Clinical trials regulations: transitional arrangements

These reports outline the MHRA’s Corporate and Business Plans, detailing the agency’s strategic direction over the next three years.

We invite feedback on the operation and impact of the human medicines and medical devices legislation as part of a statutory review required under the Medicines and Medical Devices Act 2021.

List of Field Safety Notices from 29 December 2025 to 2 January 2026.

Crescent Pharma Limited is recalling one batch of Ramipril 5 mg Capsules as a precautionary measure due to a potential error at the manufacturing site.

By Julia Vitarello

How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.