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What to do if you think you are a victim of identity theft or fraud, and what signs to look out for.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Find a BFPO number, send mail to and from British forces personnel and their families
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
FCDO travel advice for Cuba. Includes safety and security, insurance, entry requirements and legal differences.
How to show the MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidance on listed diseases of fish and shellfish and their status in England and Wales, including what happens if a disease is suspected or confirmed.
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