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
The MHRA was alerted by Beyond Compliance and the UK National Joint Registry (NJR) to a significantly higher revision rate observed with the ORIGIN PS patient-matched total knee replacement.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
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 to support commercial fishers on under 12 metre English vessels.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
A buyer's guide for mobile devices, which outlines 7 areas that consumers should check for when choosing or using their mobile device.
Information about the EU Regulations and their implementation in Northern Ireland
How to tax company mobile phones given to employees.
How to conform with the legal requirements for placing medical devices on the market.
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
Information and guidance on a range of medical devices for users and patients.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Guidance for local authorities, trusts, schools, colleges and FE institutions about who owns DfE loaned devices, asset management and loan agreements.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
What to do if a laptop or tablet you’ve received from a DfE programme is not working.
How the supply of medical devices from Great Britain into Northern Ireland works.
Information on content filtering and mobile device management to ensure devices are safe to use by young people and families
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. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.