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 a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Find the notes for all Declaration Category Data Set tables covered by Appendix 21-25 of the CDS Declaration and Customs Clearance Request Instructions.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Assess your goods, software and technology to determine whether or not they are controlled and require a licence to export.
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guide to licensing requirements and restrictions for trade control and the export of controlled military goods, software and technology.
Guidance for manufacturers, importers and distributors.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
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)’
Guidance on the content of a Development Consent Order required for a Nationally Significant Infrastructure Project.
Tax and reporting rules for employers covering the cost of employees using their own vehicles for business travel
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The information required by the Regulator of Social Housing and the deadlines for submission.
This guidance sets out the process for determining whether governance approval and ethics review is required for research undertaken, funded or sponsored by MOD.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Explains how conditions attached to a planning permission should be used and discharged effectively
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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.