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Get information on teacher training courses, funding, pay scales and how to make a great application
Renew and pay for a GB or European patent online - when renewal is due, fees, renew by post or phone instead
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Having right of abode means you're allowed to live or work in the UK without any immigration restrictions - apply for a certificate of entitlement to prove you have it.
Using metadata to make it easier to catalogue, validate, reuse and share your data.
Find the address, contact details and opening times of the UK visa application centre for your country.
Pharmacovigilance system requirements
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
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 to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Get endorsement for the Global Talent visa to work in the UK as a digital technology expert - fintech, gaming, cyber security, artificial intelligence
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Look up a trade mark to see if something identical or similar to your brand is already registered.
What you need to do to work and operate in the aviation industry.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Visit the UK as a Standard Visitor for tourism, business, study (courses up to 6 months), medical treatment and other activities. Find out whether you need a Standard Visitor visa, or can visit without a visa.
Information about the DCIA programme, with guidance on how to participate in the Pilot competition
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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