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Find out if you need to declare goods you bring into or take out of the UK and how to make the declarations.
Use these forms if you import, export, or move goods through the UK.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Check how much your visa application costs in the country you’re in
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Make sure that domains that do not send email cannot be used for spoofing.
The civil procedure rules govern the way civil cases are managed, and set out the processes of the Civil Division of the Court of Appeal, the High Court and the County Court.
Renew, replace or apply for an adult or child British passport if you’re living abroad or working overseas - forms, prices, how long it takes
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Nigeria is subject to regional controls governing small arms and light weapons.
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Short-term study visa - prepare supporting documents, apply, book and attend an appointment, what happens at the UK border
To help them carry out their duties British military personnel and visiting members of the armed forces have a number of driving exemptions.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Niger is subject to regional controls governing small arms and light weapons.
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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