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For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives in Great Britain and Northern Ireland.
The legal text underpinning the regulation of manufacture, authorisation, marketing, distribution, use and post-authorisation surveillance of veterinary medicines and medicated feed.
The legal requirements to advertise and promote your medicine including the Blue Guide which interprets the law in more detail.
Information about new applications, post-licensing, advertising, product information and fees.
Information for patients, healthcare professionals and developers of new medicines
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines
This guide is about infections that occur in people who inject drugs (PWID).
Guidance for healthcare and public health commissioners on planning treatment services for dependence on prescription and over-the-counter medicines.
Guidance on how to reclassify your medicine and how to name medicines.
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