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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.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
VAT and other taxes on shopping and services, including tax-free shopping, energy-saving equipment and mobility aids.
FCDO travel advice for Chile. Includes safety and security, insurance, entry requirements and legal differences.
The review of the safety of isotretinoin has concluded.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to get access to MHRA submissions portals, how to use them, where to go for help.
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