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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Find registered patents, patent applications and pending patents
Get information on teacher training courses, funding, pay scales and how to make a great application
Use these forms if you import, export, or move goods through the UK.
You may need a visa to come to the UK to visit, study or work.
VisitBritain (VB) is the national tourism agency, responsible for marketing Britain worldwide and developing Britain’s visitor economy. It works with UK Trade & Investment as well as airlines, travel operators, global brands and the official tourism bodies for London, England,...
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...
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.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
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.
The process of taking or giving evidence from abroad for UK court cases and rules on which countries allow it.
The Civil Aviation Authority (CAA) is responsible for the regulation of aviation safety in the UK, determining policy for the use of airspace, the economic regulation of Heathrow, Gatwick and Stansted airports, the licensing and financial fitness of airlines and...
Check what you need to do to employ teachers who are non-UK citizens.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Check the tariff classification for the unassembled parts to be implanted into the human body for different spinal treatments.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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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