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1. www.gov.uk › guidance › find-product-information-about-medicinesFind product information about medicines - GOV.UK

   www.gov.uk › guidance › find-product-information-about-medicines

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   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).

2. products.mhra.gov.ukMHRA Products | Home

   products.mhra.gov.uk

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   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...

3. assets.publishing.service.gov.uk › guide_8_what_is_a_medicinal_productA GUIDE TO WHAT IS A - GOV.UK

   assets.publishing.service.gov.uk › guide_8_what_is_a_medicinal_product

   Healthcare products Regulatory Agency (MHRA) regulates medicinal products for human use in accordance with the European Community’s medicinal products directive (Directive 2001/83/EC, as...

4. www.gov.uk › government › organisationsMedicines and Healthcare products Regulatory Agency

   www.gov.uk › government › organisations

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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...

5. www.gov.uk › guidance › medicines-packaging-labelling-and-patient-information-leafletsMedicines: packaging, labelling and patient information leaflets

   www.gov.uk › guidance › medicines-packaging-labelling-and-patient-information-leaflets

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   18 Δεκ 2014 · The MHRA approves all packaging and labelling information for medicines sold in the UK including the information that must be provided. Medicines must include a patient information leaflet...

6. assets.publishing.service.gov.uk › 872742 › GN8_FINAL_10_03_2020__combined_MHRA Guidance Note 8 - GOV.UK

   assets.publishing.service.gov.uk › 872742 › GN8_FINAL_10_03_2020__combined_

   This Guidance explains how, and on what basis, the MHRA decides whether products are medicines or not and clarifies the MHRA’s position on traditional herbal medicinal products. 2. MHRA...

7. www.consultantchemist.co.uk › 12 › MHRA-A-GUIDE-TO-WHAT-IS-A-MEDICINAL-PRODUCTA GUIDE TO WHAT IS A MEDICINAL PRODUCT - consultantchemist.co.uk

   www.consultantchemist.co.uk › 12 › MHRA-A-GUIDE-TO-WHAT-IS-A-MEDICINAL-PRODUCT

   To protect public health, and on behalf of the UK Licensing Authority, the Medicines and Healthcare products Regulatory Agency (MHRA) regulates medicinal products for human use in accordance with the European Community’s medicinal products directive (Directive 2001/83/EC, as amended, “the Directive”) and UK law.