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Use a global project licence to simplify the export of military goods and technology classed as collaborative defence projects.
Carry out checks on your overseas customers and find out what records you’ll need to keep if you’re approved for the Fulfilment House Due Diligence Scheme.
You can make observations on the patentability of a published patent application.
Southern Region, Mrs J Coupe FRICS Regional Surveyor on 18 March 2024
Information to help you protect, manage and enforce your Intellectual Property (IP) rights in South Korea.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Find out the information you must give to customers on food products and how to give it.
Start date notices, inquiry & hearing notices and rejection letters published in 2023 for rights of way orders
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
This page provides practical information to help you make the most of your IP when doing business in Kazakhstan.
Definitive fees charged for applications under Schedule 7 of the Veterinary Medicines Regulations 2013.
Check timescales for the Legal Aid Agency (LAA) to process your work (eg prior authority application, graduated fee claims).
Imposing safeguard measures for imports of certain steel products.
Information on using the app to apply for an electronic travel authorisation (ETA) to come to the UK.
The targets we set each year to measure our performance and progress.
Information for British citizens moving to or living in China, including guidance on residency, healthcare and travel.
Check if you need a visa or permit to work in the Czech Republic and how to get one if you do.
This guidance is on a Union making an application to be recognised for collective bargaining
Apply for indefinite leave to remain ('settlement') if you have a business, investor or talent visa - fees, who's eligible, how to apply.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
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