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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.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
Search reports on business payment practices: when invoices are paid, payment terms and practices
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Submission dates and how the submissions using the EC decision reliance procedure work.
How to confirm a measles diagnosis, manage cases and contacts, control infection, and vaccinate young or partially-covered patients.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Guidance for prescribing vets on the use of the cascade.
Data on the real-world efficacy of the COVID-19 vaccines.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
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