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How to import animals and animal products to Great Britain (England, Scotland and Wales), the Channel Islands and the Isle of Man from non-EU countries.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
How the MHRA assesses marketing authorisation applications (MAA) for medicines referred under Article 29.
Use these general provisions to help you determine the origin of your products.
Find out which radioactive sources you need a licence to export and how to apply for one.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Check if you need an Article 10 certificate for commercial use of endangered species on the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) list.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
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