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
Register to vote Register by 18 June to vote in the General Election on 4 July.
How you can report cases of modern slavery in the UK if you’re a first responder.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to use a quasi-experimental study to evaluate your digital health product.
Use the cloud first policy by evaluating cloud computing before other options.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This guide has been provided to reduce the burden when preparing responses to Post Inspection Letters.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to use a crossover randomised controlled trial to evaluate your digital health product.
Find out how the government chooses open standards, and how you can suggest open standards, to improve services for users.
Data First is a pioneering data-linking, research and academic engagement programme led by the Ministry of Justice and funded by ADR UK.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
We recognise that you and other members of your household might be experiencing additional stress, anxiety, or financial strains due to the current cost of living pressures. To help, we’ve created this guide on how to make sure you’re getting...
The government introduced a ‘Cloud First’ policy in 2013 for all technology decisions.
Submissions related to human medicines need to be submitted directly to the MHRA.
Patients requiring treatment outside of hospitals will be able to choose between multiple providers across the NHS and independent sector.
Apply for your first adult British passport - who can apply, how long it takes, costs, how to apply, documents you need, passport interviews
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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).