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.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
Chief Medical Officer for England, Professor Chris Whitty's annual reports and lectures on medicine and public health.
Find out about Gulf War Syndrome, research programmes, medical countermeasures and reports.
How to get state healthcare if you live, work or study in Croatia.
How to get state healthcare if you live, work or study in Austria.
Information for patients, healthcare professionals and developers of new medicines
How to get state healthcare if you live, work or study in Luxembourg.
How to get state healthcare if you live, work or study in the Czech Republic.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How investigators and sponsors should manage clinical trials during COVID-19
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices, and information about the publication of two recent Device Safety Information pages. The article also includes information on a recent National Patient Safety Alert...
How to get state healthcare if you live, work or study in Switzerland.
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).