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Did you mean ce self certification?
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to conform with the legal requirements for placing medical devices on the market.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Form and guidance on self-certification for manufacturers of video surveillance systems (VSS).
Guidance providing practical information for placing construction products on the Northern Ireland market and unfettered access provisions.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
How to place CE marking on your product, how to identify UK requirements relating to construction products, and how to apply to be a UK Notified Body or Technical Assessment Body.
Information for businesses on the regulatory framework and transitional arrangements January 2023.
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