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Use this form to file a translation in connection with a European patent or a European patent application
To protect your patent outside of the UK, you usually need to apply in each country you want protection in.
The UKSIA manages UK domestic fishing vessel access to non-UK waters and foreign vessel access to UK waters.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
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...
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
How someone in Austria can get documents legalised, witnessed or certified, take an oath, affirmation or affidavit and obtain informative notes on UK naming law
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Documents, certificates, letters and notes available at the British High Commission in Singapore.
List of administrations whose Certificate of Competency (CoC) are accepted towards issuing a UK Flag State Endorsement (FSE)
What you need to do to work and operate in the aviation industry.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Check how much your visa application costs in the country you’re in
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
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.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Find out information on the UK's tax treaties, related taxation documents and multilateral agreements.
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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