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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...
Find registered patents, patent applications and pending patents
Get information on teacher training courses, funding, pay scales and how to make a great application
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Pharmacovigilance system requirements
The Intellectual Property Office (IPO) is the official UK government body responsible for intellectual property (IP) rights including patents, designs, trade marks and copyright. IPO is an executive agency, sponsored by the Department for Science, Innovation and Technology , supported...
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Check how much your visa application costs in the country you’re in
Information about the EU Regulations and their implementation in Northern Ireland
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Export controls applying to Weapons of Mass Destruction (WMD) related activities - transfer of technology and provision of technical support
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Use this form to file a translation in connection with a European patent or a European patent application
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
What you need to do to work and operate in the aviation industry.
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
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
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