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News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Check the veterinary product information database to find out if a medicine is safe to use on your pet or has been removed from sale
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Submission dates and how the submissions using the EC decision reliance procedure work.
Guidance and support on coronavirus (COVID-19) in Scotland.
The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Legal requirement for the sale of veterinary medicines on the internet and the VMD Accredited Internet Retailer Scheme (AIRS).
Animal bites and pasteurella infections information for healthcare staff.
Guidance and support on coronavirus (COVID-19) in Wales.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Blogs where government organisations talk about their work and share information and ideas.
Current issues relating to imports and exports of animals and animal products.
Bringing pets into Great Britain: pet passports, Great Britain pet health certificates, microchipping, rabies vaccinations, travelling with assistance dogs.
Guidance and application forms for Marketing Authorisations, Animal Test Certificates, Veterinary Homeopathic Remedy, Export and Import certificates, Batch release and Batch control.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on the Specific Batch Control (SBC) scheme for release of product on to the UK market.
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
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