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Advice to Lisa Osofsky, former Director of the Serious Fraud Office, The Serious Fraud Office, on business appointments after leaving Crown service.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
VICH consultation until 15 August 2024 on guidelines relating to the technical requirements for demonstrating pharmaceutical development of veterinary medicinal products.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
An initiative for companies committed to integrating 10 corporate responsibility principles in their business operations and strategies.
Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner.
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Form L7 for the isolation, identification and toxin detection of clostridium botulinum and Staphylococcus aureus.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
Product Safety Report for Esapharma Movate Steroid Cream presenting a serious chemical risk.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
How to use a contextual inquiry when developing your digital health product.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
Form to object to an application to register a traditional term for a wine product under the UK GI scheme.
We give statutory advice to ministers on the risks to human health and the environment from the release of genetically modified organisms (GMOs). ACRE is an advisory non-departmental public body, sponsored by the Department for Environment, Food & Rural Affairs...
This series brings together all documents relating to Marine science yearbooks
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