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
What is considered off-label use of a medical device and examples of it.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Guidance on sources of electromagnetic interference and mitigating the risks.
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Hand luggage restrictions at UK airports - carry-on luggage, checked-in baggage, restricted items and liquids, electronic devices carried from Turkey, Lebanon, Egypt and Saudi Arabia
Advice on writing clear notices and maximising replies to your FSNs.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to distinguish between products that are regulated as medical devices and those regulated as medicinal products.
Links to EU guidance, as it stood immediately before end of transition period.
Some of the different symbols used on medical devices.
Checklists providing a practical guide to using medical devices.
From brussels sprouts to dodgy diet products, these tips from the MHRA will help you stay safe during the festive season and beyond
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Certificates you can use when zero rating goods or services under the VAT Act 1994, Schedule 8, Group 15, items 4 to 6.
Legal requirements and good practice guidance for SQP retailers’ premises inspections.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
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.