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The Ukraine Extension Scheme is open to some Ukrainian nationals and their family members who have, or previously had, permission to be in the UK.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Find out how the ATA Carnet works, what to do at customs, and what happens if your goods are lost, destroyed or stolen.
Driving licence exchange and rules for drivers living in the EU, Iceland, Liechtenstein, Norway or Switzerland.
Check how quickly you’ll receive a decision on your UK visa application if you're applying from inside the UK.
Information for companies on the import and export of controlled drugs to and from the UK.
The Veterinary Medicines Directorate may suspend or expire a licence to market an animal medicine if it fails to comply with the regulations.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Apply to replace a time limited licence or condition that is expiring.
Information about what it means to have indefinite leave to remain (ILR) in the UK, also known as settlement.
Renew a trade mark, including late renewals and restoring a trade mark
Guidance for businesses holding registered Community designs and international trade marks and designs.
If you've reached the maximum points allowed, find out how to remove them and avoid a further £200 penalty. Check when individual penalty points expire.
Apply for indefinite leave to remain if you have an Innovator Founder or Innovator visa - fees, who's eligible, how to apply.
Sets out the process for efficient and inclusive consultation of planning applications
Apply for a Student visa to study in the UK if you're 16 or over - eligibility, extend or switch your visa, how much it costs and how long it takes
Apply for indefinite leave to remain ('settlement') if you have a Skilled Worker, T2 or tier 2 visa - fees, who's eligible, how to apply.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Explains control of advertisement regime.
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