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Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
This series brings together all documents relating to drugs licensing.
It's illegal to drive if you're unfit to do so because you're on legal or illegal drugs, or you have certain levels of drugs or medicine in your blood
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Information about new applications, post-licensing, advertising, product information and fees.
Recommendations for a temporary class drug order on a number of methylphenidate-based novel psychoactive substances.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 April to 30 June 2024.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
This series brings together all documents relating to Alcohol and drug research and analysis
Monthly PDF editions of the Drug Safety Update newsletter from MHRA and its independent advisor, the Commission on Human Medicines
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
Diagnostic request form (S3) for HIV.
Information for prospective growers of low THC cannabis (industrial hemp), for the production of seed and fibre only.
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 .
How to renew marketing authorisations for products granted through different routes and at different times.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
Consultation to provide opportunity for drugs sector organisations and other partners to influence the development of the new drug strategy.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
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