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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).
UK Government responds to expert committee recommendations on consumer CBD products.
How the MHRA makes decisions on what is a medicinal product (borderline products).
How to apply for a traditional herbal registration (THR) to market a herbal medicine in the UK.
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
Information for patients, healthcare professionals and developers of new medicines
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
It's illegal to drive if you're unfit to do so because you're on legal or illegal drugs, or you have certain levels of drugs or medicine in your blood
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 traditional herbal medicines and homeopathic medicines will be treated by the MHRA.
In October 2001 the Home Secretary asked the Advisory Council on the Misuse of Drugs to review the classification of cannabis preparations in…
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
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