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Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Find out how to complete and submit an Other Interest (OI) return using the HMRC spreadsheet or electronic flat text file.
Guidance for haulage companies and commercial drivers moving accompanied (self-drive) RoRo freight and unaccompanied RoRo freight between Great Britain (England, Scotland and Wales) and the European Union.
Guidance explaining the export of controlled goods.
Resilient energy networks are critical for energy security, and a strengthening of our electricity network will ensure we can meet challenges from an increasing diversified energy mix.
Guidance for businesses.
Guidance for business and government departments.
Information for existing and new Universal Credit claimants with more than 2 children.
You can claim a relief to pay less Customs Duty and VAT if you re-import goods to the UK.
If both the UK and another country charge Inheritance Tax, you could avoid or reclaim the tax through a double taxation convention.
Find out when you must label your meat, fish or seafood product with its country of origin.
EU and GB domestic rules for drivers of goods vehicles and passenger-carrying vehicles
This note sets out the methodology used to develop an index of priority places for the Levelling Up Fund.
If you are moving goods into Great Britain, into Northern Ireland from Great Britain, or into Northern Ireland from outside the EU, you'll need to make an entry summary declaration.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
When to take Driver Certificate of Professional Competence (CPC) periodic training if you're a lorry, bus or coach driver, how to find courses, and what happens if you miss your deadline.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Assess your goods, software and technology to determine whether or not they are controlled and require a licence to export.
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