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Sets out when planning permission is required and different types of planning permission which may be granted.
This guidance explains the information required to complete the leaseholder deed of certificate, and what information your current landlord must provide in the landlord’s certificate.
Fill in this RMOP form to get approval from APHA to transport pets or assistance dogs to England, Scotland or Wales.
RA1, RA2, RA3, RA4, RA5 bilingual forms for completion following a drugs test in custody.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Check which documents you need to carry if you're the driver or a passenger in a lorry or other heavy goods vehicle (HGV) that crosses international borders.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Find out about safety and security requirements that apply to goods entering and exiting the UK.
The information required by the Regulator of Social Housing and the deadlines for submission.
Guidance on activities that may require a marine licence.
Information to help you identify if your organisation needs to publish a modern slavery statement.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
International regulations and required documentation for hauliers transporting dangerous or hazardous goods by road or by vehicles on ships.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Supports effective delivery of planning application process.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Provides advice on when Transport Assessments and Transport Statements are required, and what they should contain.
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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