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Register to vote Register by 18 June to vote in the General Election on 4 July.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
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.
Guidance for manufacturers, importers and distributors.
Guidance for providers, social workers and placement commissioners on placing children, subject to a deprivation of liberty order (DoL), in unregistered settings.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Find out about the rules for placing transportable pressure equipment on the market in Great Britain from 1 January 2023.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
Find out if you will need to use the new UKNI marking and how to use it.
Information about the EU Regulations and their implementation in Northern Ireland
When you must report the amount of electrical and electronic equipment (EEE) you place on the market and how to do 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
Guidance for manufacturers, their authorised representatives and importers.
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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