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.
Posters and leaflets about using medical devices safely for healthcare professionals.
The Innovative Devices Access Pathway (IDAP) pilot is designed to accelerate the development of innovative medical devices that meet an unmet clinical need in the NHS and support their integration into the UK market.
I-VMS - Frequently asked questions
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
A proactive, collaborative, agile and the first of its kind approach to identifying and addressing the challenges faced by AI as a Medical Device (AIaMD).
Information to support commercial fishers on under 12 metre English vessels.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
How schools should setup a Microsoft Windows laptop or tablet before lending the device to a child, family or young person.
When to pay tax or National Insurance on tests for COVID-19 and personal protective equipment (PPE).
Research detailing cyber security issues in internet-connected devices used by businesses and organisations.
Guidance for healthcare professionals covers the use, management and safety of in vitro diagnostic (IVD) devices, including blood glucose meters.
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
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).