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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Submission dates and how the submissions using the EC decision reliance procedure work.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
Submissions related to human medicines need to be submitted directly to the MHRA.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
This Privacy Notice explains who is processing your data, the personal data we collect, how we use it, who we share it with, and what your legal rights are.
What to do if you think you've spotted a scam pretending to be from Companies House, and examples of scam emails, letters and telephone calls.
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