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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.
To help you protect, manage and enforce your intellectual property (IP) rights in Laos.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
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...
Make sure that domains that do not send email cannot be used for spoofing.
Pharmacovigilance system requirements
Information about the EU Regulations and their implementation in Northern Ireland
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.
The process of taking or giving evidence from abroad for UK court cases and rules on which countries allow it.
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.
Check how much your visa application costs in the country you’re in
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
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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