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
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Standardisation explained.
Pandemic flu planning information for England and the devolved administrations, including guidance for organisations and businesses.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
How to use Method 2 to work out the customs value of your imported goods if you’re an importer or clearing agent.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Learn how to publish accessible documents to meet the needs of all users under the accessibility regulations.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
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.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
The DUCR and the optional Part suffix is the main reference key to any Customs Handling of Import & Export Freight (CHIEF) declaration.
Find out about the customs simplified procedure aggregation rules for the Customs Declaration Service (CDS).
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.
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. Please fill in this survey (opens in a new tab).