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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.
MHRA updates product information regarding the very rare risk of non-arteritic anterior ischemic optic neuropathy (NAION) in patients taking semaglutide.
Information on comparator products used in studies supporting abridged marketing authorisation application.
As with any medicine, the MHRA will keep the safety and effectiveness of lenacapavir under close review.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
Guidance on conditional marketing authorisations, exceptional circumstances marketing authorisations and national scientific advice.
Guidance on using non-investigational medicinal products in a clinical trial.
Guidance for prescribing vets on the use of the cascade.
How authorised veterinary medicines, products supplied under the cascade and products used under the Veterinary Medicines Internal Market Scheme and Veterinary Medicines Health Situation Scheme can be advertised.
There are changes to the legislation on reference medicinal products (RMPs) used to support abridged marketing authorisation applications.
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