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Find the address, contact details and opening times of the UK visa application centre for your country.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Make sure that domains that do not send email cannot be used for spoofing.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Add metadata to data you are publishing so search engines can find the data you’ve published and display structured results for users.
Use this form to file a translation in connection with a European patent or a European patent application
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Calculate value build-up costs for use with the Single Administrative Document (SAD) using form C89.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
Development of a standard approach for AI and autonomy in networked multi-sensor systems in security and defence.
How to self-upload evidence when making an application to come to or stay in the UK.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Get endorsement and approval to apply for the Global Talent visa to work in the UK as a leader in arts and culture - architecture, fashion, film, television.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Publish your code and use open source to improve transparency, flexibility and accountability.
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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