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 apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to use a randomised controlled trial to evaluate your digital health product.
Submissions related to human medicines need to be submitted directly to the MHRA.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Learn how to check if your website or mobile app is accessible.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Working with others to embed the importance of place within the published guidance.
Emerging techniques on how to prevent or minimise the environmental impacts of post-combustion carbon dioxide capture.
Helping public health practitioners conducting evaluations – developing a logic model to represent how your intervention works.
Check the tariff classification for vitamin gummies.
FCDO travel advice for Chad. Includes safety and security, insurance, entry requirements and legal differences.
The epidemiology, symptoms, diagnosis and management of human T-cell lymphotropic virus types 1 and 2 (HTLV-1 and HTLV-2).
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
These draft regulations set out the additional conditions that expenditure by employers on recommended medical treatment must meet in order to qualify for the tax exemption at section 12 of Finance Act 2014.
Get endorsement for the Global Talent visa to work in the UK as a digital technology expert - fintech, gaming, cyber security, artificial intelligence
The recommended environmental management system (EMS) designed to achieve the general objectives of the OSPAR Offshore Strategy.
The review of the safety of isotretinoin has concluded.
Rules for UK and EU broadcasters and video on-demand services
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.