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
Information about the pre-sentence report pilot in 15 magistrates’ courts.
A summary of the types of scientific advice available at the MHRA, the process for getting advice and the fees involved.
PLIM: an approach to ensuring the relationship between prompts and large language models is validated quickly and efficiently.
Information on measures introduced by the government to tackle late and unfair payment practices in both public and private sectors.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The Medicines and Healthcare products Regulatory Agency (MHRA) offer a pre-submission service before applying for medicines Marketing Authorisations.
How to use a quasi-experimental study to evaluate your digital health product.
Register for the PRE service to view recordings of pre-recorded evidence before trial.
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 and requires JavaScript).