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How to conform with the legal requirements for placing medical devices on the market.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
This guidance is an introduction to the Open Document Format (ODF) standard and how you can select ODF-compliant solutions.
Guidance for manufacturers, importers and distributors.
Find out about other simplifications you can apply for with consignor or consignee status.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
A list of 10 criteria that represent good practice in creating, applying and enforcing design codes.
The certificate of conformity ensures the free movement of goods and must be supplied to the buyer of a new vehicle when the vehicle is delivered.
Information for businesses on the regulatory framework and transitional arrangements January 2023.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
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.
Guidance providing practical information for placing construction products on the GB market.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
How transit can help you move goods through customs and where you can use transit to move goods to.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
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