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.
UK Statements delivered on 22 and 23 May 2024 at the WTO General Council in Geneva.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to use a quasi-experimental study to evaluate your digital health product.
How to use an interrupted time series to evaluate your digital health product.
Apply for the Registered Traveller service to get through UK border control faster and without filling in a landing card
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Upper Tribunal Administrative Appeals Chamber decision by Judge Church on 29 April 2024
Using an ecological momentary assessment to evaluate your digital health product.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This guide sets out who has to apply for a permit, how to apply and explains the other rules covering travel to Antarctica.
How to use a before-and-after study to evaluate your digital health product.
Climate change is happening and is due to human activities; along with warming, many other changes are occurring such as melting polar ice, rising sea levels and more frequent floods, droughts and heatwaves.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Signs that may suggest rabies in bats, what to do if you spot them and measures to prevent exposing yourself to the disease.
Guidance for manufacturers, importers and distributors.
Apply for a High Potential Individual (HPI) visa if you've been awarded a qualification by an eligible university in the last 5 years - eligibility, fees, documents, switch, bring your partner and children
Submissions related to human medicines need to be submitted directly to the MHRA.
Documents, certificate, letters, and notes available from the British embassy and consulates in the USA.
How to use a crossover randomised controlled trial to evaluate your digital health product.
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).