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Apply for a certificate to confirm that you only need to pay UK National Insurance contributions if you're a self-employed individual working temporarily in an EU country, Gibraltar, Iceland, Liechtenstein, Norway or Switzerland.
When and how to account for VAT when you transfer a business as a going concern (TOGC).
Find out about changes to the deemed domicile rules for Income Tax and Capital Gains Tax from 6 April 2017.
How to object to the registration of a lasting or enduring power of attorney - including forms and fees
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
This page provides practical information to help you make the most of your IP when doing business in Kazakhstan.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Look up a trade mark to see if something identical or similar to your brand is already registered.
How someone in Latvia can get documents prepared, witnessed or certified, take an oath of British citizenship and obtain informative notes.
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
How to check if your criminal record will affect your licence application, and the information you need to provide for our criminality checks.
How to remove an overseas entity's registration from the Register of Overseas Entities.
The process of taking or giving evidence from abroad for UK court cases and rules on which countries allow it.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
Check how much your visa application costs in the country you’re in
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
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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