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How to obtain an authorisation to wholesale veterinary medicines.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
How UK persons’ trading interests are protected and when authorisations must be obtained to trade with countries subject to specific extraterritorial laws.
A guide to the main academy funding, finance and governance terms and acronyms.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Pharmacovigilance system requirements
We’re working to help people securely prove who they are without having to rely on physical documents.
Register as a manufacturer, importer or distributor of active substances for use in veterinary medicines.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out about the different simplified declarations for imports and what you need to do to get authorisation to use them.
Requirements for excise goods held in duty suspension in a warehouse by an authorised warehousekeeper, registered owner, duty representative or registered consignor in the UK.
Guidance on the use of the sensitive words accreditation, accredit, accredited and accrediting, in a company, Limited Liability Partnership or business name.
Use form OS AP07 to appoint a person authorised to accept service of documents in respect of a UK establishment.
Find out if you’re a trust or company service provider who needs to register for supervision with HMRC under the money laundering regulations.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
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