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Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Use these forms if you import, export, or move goods through the UK.
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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.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Pharmacovigilance system requirements
What you need to do to work and operate in the aviation industry.
How someone in Latvia can get documents prepared, witnessed or certified, take an oath of British citizenship and obtain informative notes.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Use this form to file a translation in connection with a European patent or a European patent application
Information on how to revalidate a UK CoC (and UK GMDSS at the same time).
Use a separate statement of objection form for each Japanese GI product name you object to.
The National Archives is the official archive and publisher for the UK government and for England and Wales. It is the guardian of some of our most iconic national documents, dating back over 1,000 years. The National Archives is a...
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
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.
Check the tariff classification for the unassembled parts to be implanted into the human body for different spinal treatments.
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