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Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
Use these general provisions to help you determine the origin of your products.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
The Intellectual Property Office offers different methods of accelerating the processing of your patent application.
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
Get help to classify footwear and parts of footwear for import and export.
This document contains information about Cuba to help HM Passport Office staff process passport applications.
The Victoria and Albert Museum (V&A / VAM) is the world’s largest museum of decorative arts and design, housing a permanent collection of over 4.5 million objects. Named after Queen Victoria and Prince Albert, it was founded in 1852, and...
Information about the UK food chain.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
When to exclude and include the buying commission in the customs value and account for import VAT if you’re an importer paying fees to your buying agent.
Get help to classify ceramic articles for import and export.
Consumer advice and details of how to report problems with e-cigarettes with guidance on how to place an e-cigarette on the market in Great Britain and Northern Ireland, including the notification scheme.
Get help to classify various types of wood for import and export.
Guidance for using automated grading techniques for beef carcase classification
Obligated packaging producers must register and meet their waste packaging recycling responsibilities.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
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