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These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Guidance on the collection, verification, and reporting of safety events in clinical trials of an investigational medicinal product.
Accord Healthcare Ltd is recalling a batch of Ipratropium Bromide 500 microgram/2ml Nebuliser Solution after a foil pouch was found to contain ampoules with incorrect labels intended for the Korean market. The incorrectly labelled ampoules are the same product and...
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
Hikma Farmacêutica (Portugal) S.A has informed the MHRA that the Patient Information Leaflet (PIL) contained within batch CB0033 of Gemcitabine 2g/52.6ml concentrate for solution for infusion does not contain the side effects of serious skin reactions.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
The Medicines and Healthcare products Regulatory Agency has approved the medicine flortaucipir (Tauvid), given to adults with memory problems so that doctors can perform a type of brain scan called a PET.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 January to 31 March 2025.
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