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Guidance for businesses holding registered Community designs and international trade marks and designs.
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
What blood establishments, blood banks and manufacturers of blood products need to do to ensure the safety and quality of blood and blood products.
Steps to take if you want to provide a service or set up a business in the UK.
Guidance on UK and EU copyright protection for right holders and users including business, cultural heritage institutions and consumers. It is not legal advice.
How to get state healthcare if you live, work or study in Luxembourg.
Advice for manufacturers and retailers on footwear labelling.
Government is calling on industry to submit their interest in piloting the Ecosystem of Trust concept that was outlined on our 2025 UK Border strategy.
List of companies working as approved bodies and designated bodies in the UK under the Railways (Interoperability) Regulations 2011.
List of visas showing their old names and their current names.
This guidance explains the rights of European Economic Area (EEA) and Swiss citizens to access social housing and homelessness assistance in England.
Information for applicants to the EU Settlement Scheme on how refunds are processed if you paid an application fee.
Guidance on exporting or moving high-risk food and feed of non-animal origin (HRFNAO) from Great Britain to the EU or Northern Ireland.
What businesses need to do to import ‘relevant’ nuclear materials into the UK.
How to get state healthcare if you live, work or study in Estonia.
Find out what you need to do if you hold a .eu domain or want to register one.
Customers must no longer access programmes via EU satellite broadcasting services to avoid a charge for a UK service.
Webinars on changes to importing food and drink, including composite food and fishery products from the EU to Great Britain.
Guidance for businesses and organisations on the relationship between trade marks and geographical indications (GIs) at the end of the transition period.
Supplementary information for international regulators on packaging changes and the export of UK medicines.
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