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Find out how you can process or store similar free circulation goods in place of goods that you have declared to the UK Freeport customs special procedure.
Find out what you can do with your goods when they are being processed or repaired using inward processing.
How to serve legal documents overseas and take evidence abroad.
How to use Method 2 to work out the customs value of your imported goods if you’re an importer or clearing agent.
How to work out the customs value of imported goods if you’re claiming inward or outward processing relief.
Find out how to declare that your goods have been put to their authorised use, destroyed or re-exported.
Supports effective delivery of planning application process.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
The DUCR and the optional Part suffix is the main reference key to any Customs Handling of Import & Export Freight (CHIEF) declaration.
Use inward processing to delay or reduce import duties or VAT on goods that you process or repair.
Guidance on identical returns for Self Assessment Online software developers.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
The process for the simultaneous review of veterinary medicine submissions by Switzerland’s Swissmedic and the UK's Veterinary Medicines Directorate.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
This is a work sharing model for the co-ordinated assessment of a generic application that has been filed with multiple Access Consortium agencies.
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
Biotechnological inventions
The process for the simultaneous review of veterinary drug submissions by Health Canada’s Veterinary Drugs Directorate and the UK's Veterinary Medicines Directorate.
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