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
A new database of Areas of Research Interest has been developed by the Government Office for Science and the Economic and Social Research Council.
Licensing bodies and collective management organisations can agree licences with users on behalf of owners and collect any royalties the owners are owed.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
This guidance provides information on COVID-19 in homelessness, domestic abuse refuge, respite room and asylum seeker accommodation settings.
What packaged goods are, how they are labelled, units of measurements used and compliance with weights and measures regulation.
Using an ecological momentary assessment to evaluate your digital health product.
Information on how the CMA investigated the merger, and how you can find out more.
Get help to classify drones and aircraft parts for import and export.
Information on trade sanctions, arms embargoes and trade restrictions, including trade controls, transit controls and restrictions on terrorist organisations.
FCDO travel advice for Aruba. Includes safety and security, insurance, entry requirements and legal differences.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Guidance for manufacturers, importers and distributors.
How to minimise your risk, and what to do if there's a terrorist attack.
Find out if the goods you're declaring to inward or outward processing are classed as sensitive goods.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a cost utility analysis to evaluate your digital health product.
How the Valuation Office Agency calculates your rateable value for business rates.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
The prohibitions and restrictions on the import of animal furs and skins into the UK and the export of salmon and trout.
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).