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Register to vote Register by 18 June to vote in the General Election on 4 July.
Information for patients who have been prescribed Paxlovid (nirmatrelvir 150mg and ritonavir 100mg) film-coated tablets COVID-19 antiviral medication.
Exeltis UK Limited has informed the MHRA regarding an inconsistency in the Patient Information Leaflet (PIL) packaged in cartons of the specified batches of Gepretix 100mg capsules.
Information for healthcare professionals, patients, and the public.
How veterinary medicines can be advertised.
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
Requirements for an Animal Test Certificate (ATC) to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Information for those who have been prescribed Paxlovid.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
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