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The Foreign, Commonwealth & Development Office (FCDO) provides lists of English-speaking lawyers abroad to help British nationals find the legal support they need.
Details of General Licences issued by OFSI
Website of Cumberland Council
You must fill in this form to confirm that you won't sell or transfer the pet dog, cat, ferret or assistance dog to a new owner in the UK.
List of fees for consular information in the USA.
Renew and pay for a GB or European patent online - when renewal is due, fees, renew by post or phone instead
List of Field Safety Notices from 22 to 26 April 2024.
Use these forms if you import, export, or move goods through the UK.
Find out about changes to the deemed domicile rules for Income Tax and Capital Gains Tax from 6 April 2017.
We pursue our national interests and those of British citizens. We safeguard the UK’s security, defend our values, reduce poverty and tackle global challenges with our international partners. FCDO is a ministerial department, supported by 12 agencies and public bodies...
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Find out how to link your temporary storage facility to Customs Handling of Import and Export Freight (CHIEF) or the Customs Declaration Service using a Community Systems Provider.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
Check the tariff classification for flavour pods.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
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