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Interim guidance and information on the law for healthcare professionals
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
The legal text underpinning the regulation of manufacture, authorisation, marketing, distribution, use and post-authorisation surveillance of veterinary medicines and medicated feed.
Adapt this example letter to give evidence of a Multi-agency Risk Assessment Conference protection plan (for victims of domestic violence).
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.
Information for patients, healthcare professionals and developers of new medicines
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Apply to be an authorised animal feedingstuffs manufacturer and/or distributor.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This series brings together all documents relating to ACMD correspondence.
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