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Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
How the MHRA makes decisions on what is a medicinal product (borderline products).
Information about new applications, post-licensing, advertising, product information and fees.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Information for patients, healthcare professionals and developers of new medicines
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
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