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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
When you need building regs approval, how to apply, using a competent person scheme, and determinations and appeals
How the Office for Product Safety and Standards contributes to the national regulatory landscape.
The Regulatory Policy Committee provides the government with external, independent scrutiny of the evidence supporting changes in law that affect businesses, charities and community groups.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
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.
Keep up to date with the latest information from the UK GLP monitoring authority.
What is involved in regulatory judgements and gradings
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Concise, principles-based core competencies for regulators and people training as regulators.
Standardisation explained.
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