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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.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
Check how much your visa application costs in the country you’re in
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
What you need to do to work and operate in the aviation industry.
Defence Standardization develops and pursues MOD’s standardization policy, both nationally and internationally, with civil and military partners to support increased interoperability and more effective acquisition.
Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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.
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.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
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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