We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
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 to use Method 2 to work out the customs value of your imported goods if you’re an importer or clearing agent.
Ahead of a huge summer of sport in 2024, schools will receive new guidance on delivering two hours of PE a week, and equal access to sport and PE.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out how you can process or store similar free circulation goods in place of goods that you have declared to the UK Freeport customs special procedure.
Learn how to publish accessible documents to meet the needs of all users under the accessibility regulations.
How to link charities to make accounting and reporting easier.
Foreign, Commonwealth & Development Office (FCDO) advice for lesbian, gay, bisexual and transgender (LGBT+) people travelling abroad.
Find out how to prove the originating status of your goods and check if you can claim preferential tariff treatment.
How the MHRA processes variations to Marketing Authorisations (MAs)
Guidance for businesses and organisations holding EU trade marks at the end of the transition period.
How to apply for marketing authorisation via this new procedure.
The DUCR and the optional Part suffix is the main reference key to any Customs Handling of Import & Export Freight (CHIEF) declaration.
Pharmacovigilance system requirements
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
What cattle keepers must record and report when they move cattle, bison or buffalo and the deadlines.
You can claim a relief to pay less Customs Duty and VAT if you re-import goods to the UK.
Supports effective delivery of planning application process.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
How to use a randomised controlled trial to evaluate your digital health product.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.