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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.
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.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Pharmacovigilance system requirements
Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
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