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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...
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About this service SPC-PILs. Patient information leaflet...
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Our ninth annual #MedSafetyWeek campaign runs from 4 to 10...
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The Medicines and Healthcare products Regulatory Agency (MHRA) has approved eplontersen (Wainzua) to treat adults with polyneuropathy associated with hereditary transthyretin amyloidosis (ATTRv),...
18 Δεκ 2014 · Medicines, medical devices; Marketing authorisations, variations and licensing guidance
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.
Guidance explains how, and on what basis, the MHRA decides whether products are medicines or not. It includes guidance on the review procedures in Part 9 of the Regulations. This latest version...
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK.
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...