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As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
Check the tariff classification for a defined daily dose of active substances.
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Guidance for prescribing vets on the use of the cascade.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
How to confirm a measles diagnosis, manage cases and contacts, control infection, and vaccinate young or partially-covered patients.
Data on the real-world efficacy of the COVID-19 vaccines.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Comprehensive information on the change to the HPV programme from September 2014.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
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