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 local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
Information about the EU Regulations and their implementation in Northern Ireland
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Information and guidance on a range of medical devices for users and patients.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to get fast-track approval of medical devices during COVID-19.
Using an ecological momentary assessment to evaluate your digital health product.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
Advice on writing clear notices and maximising replies to your FSNs.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
Information about who could get devices from the Get Help with Technology programme and how devices were allocated to disadvantaged children and young people.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to conform with the legal requirements for placing medical devices on the market.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
Licensing bodies and collective management organisations can agree licences with users on behalf of owners and collect any royalties the owners are owed.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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).