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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to conform with the legal requirements for placing medical devices on the market.
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Information about applying for a review of marking for key stage 2 (KS2) national curriculum tests.
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What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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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.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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