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The Medicines and Healthcare products Regulatory Agency (MHRA) has today, 23 October 2024, approved a licence for the medicine donanemab (Kisunla) for use in the early stages of Alzheimer’s...
The MHRA products website allows you to find: The leaflets which are provided with medicines. The description of the medicinal product’s properties and how it can be used. Scientific reports...
19 Δεκ 2019 · Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
18 Δεκ 2014 · Parallel import licences: lists of approved products; Immunomodulatory drugs: temporary pregnancy prevention guidance during coronavirus (COVID-19) Find product information about medicines
The Medicines and Healthcare products Regulatory Agency (MHRA) is an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe.
Up to date, approved and regulated prescribing and patient information for licensed medicines
Once a drug has authorisation, it is 'licensed' or 'approved'. All these terms mean the same thing. Go to more information about the MHRA on the GOV.UK website. The MHRA works with other medicines regulators in certain countries around the world.