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This guide is about infections that occur in people who inject drugs (PWID).
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
You must get permission to export certain drugs and medicines.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Licence and registration application information for companies that deal in precursor chemicals.
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Don’t include personal or financial information like your National Insurance number or credit card details.
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