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Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
List of fees for consular information in the USA.
Having right of abode means you're allowed to live or work in the UK without any immigration restrictions - apply for a certificate of entitlement to prove you have it.
Make sure that domains that do not send email cannot be used for spoofing.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Information for British citizens moving to or living in China, including guidance on residency, healthcare and travel.
Check how much your visa application costs in the country you’re in
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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...
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
You must tell DVLA if you have a brain abscess, cyst or encephalitis - download the correct form to let them know
Use this form to file a translation in connection with a European patent or a European patent application
How to self-upload evidence when making an application to come to or stay in the UK.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Find details of recent trade mark applications or amendments by searching the journal
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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