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What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Find out which stocks and shares you can purchase, make or hold in an investor's stocks and shares ISA.
Guidance providing practical information for placing construction products on the GB market.
How the Youth Custody Service places a young person in custody, and how to question a placement decision.
Find out which standards and regulations apply to your product and how to make sure you follow the right procedures.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
A list of upcoming webinars on the UK’s approach to product marking and placing products on the market in Great Britain and Northern Ireland.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Find out about the rules for placing transportable pressure equipment on the market in Great Britain from 1 January 2023.
Guidance for providers, social workers and placement commissioners on placing children, subject to a deprivation of liberty order (DoL), in unregistered settings.
You can reserve books and other items such as DVDs at your local library - contact your council for more information
How to carry out a flood risk assessment so that you can complete your planning application.
When you must report the amount of electrical and electronic equipment (EEE) you place on the market and how to do it.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Find out if you will need to use the new UKNI marking and how to use it.
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 to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
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