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Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Guidance for healthcare professionals who complete medical reports for DWP or one of its assessment providers.
Details of the system for reporting adverse drug reactions from medicines or adverse incidents with medical devices in the UK.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Use this guidance if you are a doctor or psychologist writing a medical report for a patient’s Gender Recognition Certificate application.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
How to write up and share your findings
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