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How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Check how much your visa application costs in the country you’re in
What you need to do to work and operate in the aviation industry.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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...
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
This page provides practical information to help you make the most of your IP when doing business in Kazakhstan.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Order birth, adoption, marriage, civil partnership and death certificates from the General Register Office (GRO) - find GRO index numbers
Read about businesses that have participated in support schemes funded by the UK government.
We are here to make digital government simpler, clearer and faster for everyone. GDS is part of the Cabinet Office .
Find out how to import timber and wood material, including the documents, identity checks and plant health inspections required.
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
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
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