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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.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (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.
Find out if you will need to use the new UKNI marking and how to use it.
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