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.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Information on how to request assistance from NSDR.
Help available and steps you should take if you have a medical emergency or are hospitalised abroad, including for planned treatment.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Search reports on business payment practices: when invoices are paid, payment terms and practices
Your rights and security searches, body scans and privacy rules if you're disabled or taking medication aboard aircraft
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices, and information about the publication of two recent Device Safety Information pages. The article also includes information on a recent National Patient Safety Alert...
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Eligible health and social care providers can order PPE through the portal to meet the increased need that has arisen as a result of the COVID-19 pandemic.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Information for healthcare professionals on how pulse oximeters are regulated, home use and issues to look out for when using the devices
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How investigators and sponsors should manage clinical trials during COVID-19
Advice for manufacturers of Class I medical devices for placing products on the UK market
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.
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).