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Register to vote Register by 18 June to vote in the General Election on 4 July.
Regulators must use this process guidance note (PGN) to assess applications and write permits for the formulation and finishing of pharmaceutical products
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
Upper Tribunal Administrative Appeals Chamber decision by Judge Wright on 26 March 2024.
This study explores the structural properties of the ERG22+ formulation tool (Her Majesty’s Prison and Probation Service, 2011) which is used in the management of extremist offenders by the criminal justice system of England and Wales.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
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