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Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Find out how to declare that your goods have been put to their authorised use, destroyed or re-exported.
How the MHRA processes variations to Marketing Authorisations (MAs)
Check if you can apply for Authorised Use relief to reduce your payments when you import goods for a specific use. This can include repairs, maintenance or processing.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Find out about gaining approval for a fair partial exemption special method if you deal with partial exemption for insurers.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Find out how to give or view an authority to use deferment, guarantee or cash account to import goods.
Find out about the different simplified declarations for imports and what you need to do to get authorisation to use them.
How to apply for marketing authorisation via this new procedure.
Find out how you can import goods with a specific authorised use and pay less duty.
Find out the different ways you can get client authorisation including the digital handshake, Online Agent Authorisation service, paper forms and through your client's business tax account.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
How to use Method 1 to work out the customs value of your imported goods if you're an importer or clearing agent.
Apply for an authorisation to manufacture extemporaneous preparations, autogenous vaccines, stem cell products or blood products for non-food animals.
This guidance sets out how the MHRA is handling centralised applications that were still pending on 1 January 2021.
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