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Register to vote Register by 18 June to vote in the General Election on 4 July.
Find out what you need to do when importing commercial goods into Great Britain in your accompanied baggage or small vehicle.
Contains the statement of changes within immigration rules (1994 to 2024), codes of conduct, guidance on competence, OISC regulations and much more.
The Competition and Market Authority (CMA)'s work aims to tackle potentially harmful online selling practices.
Information about the EU Regulations and their implementation in Northern Ireland
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
The RPC is the independent regulatory scrutiny body for the UK Government. The Committee assesses the quality of evidence and analysis used to inform government regulatory proposals. This independent advice and scrutiny helps ensure that ministerial policy decisions are based...
Raft of voices below have thrown their support behind Act protecting children from online harm, while empowering adults with more choices over what they see online.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Regulatory Policy Committee opinion on DCMS' Online Safety Bill
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
BRDO is working towards a regulatory environment in which businesses have the confidence to invest and grow and citizens and communities are properly protected. We do this by operating Primary Authority to ensure consistent regulation, improving the professionalism of front-line...
Information and advice for businesses on how to comply with consumer protection law in the online reviews and endorsements sectors.
The controls that apply if you transport waste out of or into England.
What UK digital services providers must do to comply with the regulations covering the security of network and information systems.
Information for prospective growers of low THC cannabis (industrial hemp), for the production of seed and fibre only.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to file an update statement for an overseas entity and its beneficial owners or managing officers.
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.
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