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The UK's regulatory framework for strategic export controls and the circumstances where you might need an export licence.
This page provides practical information to help you make the most of your IP when doing business in Kazakhstan.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Information about the EU Regulations and their implementation in Northern Ireland
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Renew and pay for a GB or European patent online - when renewal is due, fees, renew by post or phone instead
Pharmacovigilance system requirements
Information for manufacturers.
Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
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).
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
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.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
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