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International trade mark registrations protected in the EU under the Madrid Protocol will no longer enjoy protection in the UK after 1 January 2021.
Find out if you will need to use the new UKNI marking and how to use it.
How to conform with the legal requirements for placing medical devices on the market.
Guidance for businesses and organisations holding EU trade marks at the end of the transition period.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to remove an overseas entity's registration from the Register of Overseas Entities.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Guidance on how to prove someone’s identity or give them access to your service or organisation.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
Depending on the objection raised in your examination, you have 2 months to respond through a number of options.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Section last updated: January 2019.
What packaged goods are, how they are labelled, units of measurements used and compliance with weights and measures regulation.
We have increased the checks on addresses provided in trade mark applications and introduced a process for reporting misconduct by unregulated agents.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Good Practice Guide (GPG) 44 helps you choose the authenticator that will give you the right level of protection for your service.
Don’t include personal or financial information like your National Insurance number or credit card details.
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