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
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
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 for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information about the EU Regulations and their implementation in Northern Ireland
How to conform with the legal requirements for placing medical devices on the market.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Advice for manufacturers of Class I medical devices for placing products on the UK market
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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.
Information about the qualifications available under the statutory digital entitlement.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
Information to support commercial fishers on under 12 metre English vessels.
An overview of the work the IPO is undertaking in relation to Standard Essential Patents.
I-VMS - Frequently asked questions
Millions invested in eight innovative companies behind lifesaving new medical technology which could destroy liver cancer tumours, detect Alzheimer’s and quickly spot those at risk of stroke
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).