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
Get help to classify various items of iron and steel, primarily those classified under chapter 72.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Get help to classify articles of leather and other items in chapter 42 of the tariff for import and export.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guidance on managing and using bed rails safely.
This guidance specifies the standards for the continuous monitoring and sampling of stack emissions.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
List of Field Safety Notices from15 to 19 April 2024.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance for healthcare professionals on infection control and clinical aspects of M. chimaera infection associated with cardiopulmonary bypass.
Information and guidance on a range of medical devices for users and patients.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
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.