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
First published during the 2019 to 2022 Johnson Conservative government
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Help available and steps you should take if you have a medical emergency or are hospitalised abroad, including for planned treatment.
The Defence Medical Services (DMS) comprises personnel from the Royal Navy Medical Service, Army Medical Service, the Royal Air Force Medical Service and the Headquarters Defence Medical Services (HQ DMS).
The Medicines and Healthcare products Regulatory Agency (MHRA) has designated two new UK Approved Bodies, delivering increased capacity for the certification of the performance and safety of medical devices, for healthcare professionals and the public.
Information for healthcare professional about medical education and other resources related to health and work.
First published during the 2022 to 2024 Sunak Conservative government
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Employment Tribunal decision.
The MHRA is reviewing its approach to engagement with healthcare professionals to improve the safety of medicines and medical devices.
List of medical facilities in Colombia
This quarterly report is a subset of the annual information and presents information on Patients, General Practitioners and GP Practices in NI for quarter 1 of 2024/25.
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
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).