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1. 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...

   • About This Service

     About this service SPC-PILs. Patient information leaflet...

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     Our ninth annual #MedSafetyWeek campaign runs from 4 to 10...

2. www.gov.uk › government › publicationsUK-wide licensing for human medicines - GOV.UK

   www.gov.uk › government › publications

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   30 Αυγ 2024 · From 1 January 2025, the MHRA will regulate medicines through UK-wide marketing authorisations (MAs). Any authorisation issued on or after this date, will have an MA number with a PL prefix.

3. 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).

4. www.gov.uk › guidance › converting-centrally-authorised-products-caps-to-ukConverting Centrally Authorised Products (CAPs) to UK Marketing...

   www.gov.uk › guidance › converting-centrally-authorised-products-caps-to-uk

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   31 Δεκ 2020 · Guidance. Converting Centrally Authorised Products (CAPs) to UK Marketing Authorisations (MAs), 'grandfathering' and managing lifecycle changes. This guidance covers ‘grandfathering’ and managing...

5. www.pharmacopoeia.com › how-to-use-the-bpHow to use the BP - British Pharmacopoeia

   www.pharmacopoeia.com › how-to-use-the-bp

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   How to use the BP. Download PDF version. The BP is the only comprehensive collection of authoritative official standards for UK pharmaceutical substances and medicinal products. It contains all texts and monographs of the European Pharmacopoeia (signposted with a chaplet of stars), as well as the national standards developed by the BP.

6. www.pmcpa.org.uk › media › 3322Updates to prescribing information for centrally approved...

   www.pmcpa.org.uk › media › 3322

   The MHRA guidance refers to the automatic conversion of CAPs into MAs effective in Great Britain (GB) only and issued with a GB MA number on 1 January 2021. This is referred to as ‘Grandfathering’ and these UK MAs are referred to as ‘converted EU MAs’.

7. 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...