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Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Work out the VAT liability of goods and services supplied by health and care institutions and providers of non residential care to children.
Submission dates and how the submissions using the EC decision reliance procedure work.
Guidance for manufacturers and distributors of premixtures and feedingstuffs containing veterinary medicines or specified feed additives.
Blogs where government organisations talk about their work and share information and ideas.
Get help to classify cigarettes, cigars, raw tobacco, smoking tobacco, tobacco for heating and nicotine substitutes for import and export.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Check for listed disinfectants for aquaculture; or apply to have your product listed.
Details of General Licences issued by OFSI
Use a separate statement of objection form for each Japanese GI product name you object to.
Check if you need a tuberculosis (TB) test to support your visa application and find an approved clinic in your country
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.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Submissions related to human medicines need to be submitted directly to the MHRA.
Find news, information and advice from the government on starting or growing your business.
Apply for a higher education course, track your application and accept or reject your offers.
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