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• CE marking

  How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.

  • Updated: 17 May 2024
• Medical devices: conformity assessment and the UKCA mark

  How to conform with the legal requirements for placing medical devices on the market.

  • Updated: 31 December 2020
• UKCA marking: conformity assessment and documentation

  How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.

  • Updated: 17 May 2024
• Guidance on Class I medical devices

  Advice for manufacturers of Class I medical devices for placing products on the UK market

  • Updated: 1 July 2023
• Regulating medical devices in the UK

  What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.

  • Updated: 17 February 2025
• IEIM403140 - Due Diligence: New Individual Accounts: Self Certifications
  • Updated: 29 January 2021
• IEIM404880 - Charities: Due diligence: Self-certification
  • Updated: 29 January 2021
• EU Construction Products Regulation and CE marking, including UK product contact point for construction products

  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.

  • Updated: 26 February 2025
• Certificate of free sale for exporting medical devices

  How to apply for a certificate of free sale to export medical devices outside the UK.

  • Updated: 13 March 2025
• Using the UKNI marking

  Find out if you will need to use the new UKNI marking and how to use it.

  • Updated: 3 October 2023