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The Royal Mint (RM) is the world’s leading export mint, making coins and medals for an average of 60 countries every year. However, its first responsibility is to make and distribute United Kingdom coins as well as to supply blanks...
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
List of fees for consular information in the USA.
Postgraduate funding for overseas students studying in the UK: types of scholarship, eligibility, how to apply
Website of Cumberland Council
Find registered patents, patent applications and pending patents
Use these forms if you import, export, or move goods through the UK.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Check how much your visa application costs in the country you’re in
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Renew, replace or apply for an adult or child British passport if you’re living abroad or working overseas - forms, prices, how long it takes
The National Archives is the official archive and publisher for the UK government and for England and Wales. It is the guardian of some of our most iconic national documents, dating back over 1,000 years. The National Archives is a...
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Use these EU country codes, VAT numbers and foreign language letters to complete an EC Sales List (ESL).
Look up a trade mark to see if something identical or similar to your brand is already registered.
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.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
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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