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News stories, speeches, letters and notices
Detailed guidance, regulations and rules
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Data, Freedom of Information releases and corporate reports
Decision for applicant British Broadcasting Corporation against registration number 14988089, applicant successful.
Decision for applicant Jamie Oliver Enterprises Limited against registration number 15369357, applicant successful.
Decision for applicant Bugatti International S.A. against registration number 14624080, applicant successful.
Information about the LEO dataset including guidance, research reports and official statistics.
Employment Appeal Tribunal Judgment of Lord Stuart on 8 April 2024.
Employment Appeal Tribunal Judgment of Mrs Justice Eady on 18 April 2024.
Employment Appeal Tribunal Judgment of Judge Tayler on 12 April 2024.
Check if your import, export or re-export needs a permit or certificate under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES).
Guidance for those affected by changes to UK immigration and borders due to coronavirus.
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
Use a separate statement of objection form for each Japanese GI product name you object to.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
How to spot dourine, what to do if you suspect it and measures to prevent its spread.
How to object to an application to use or change a traditional term for a wine product on the UK traditional terms register.
Form to object to an application to register a traditional term for a wine product under the UK GI scheme.
Definitions for terms used in Regulating the Standards
Guidance on how to apply to access the LEO standard extract through the Office for National Statistics secure research service.
Information on variants of the SARS-CoV-2 virus.
Change or cancel a UK registered traditional term for a wine product and how to appeal a decision.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
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