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 get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How to create a model of how your digital health product works and choose measures for your evaluation.
What you need to know about and do to comply with the law and keep consumers safe.
How to use a micro-randomised trial to evaluate your digital health product.
How to write up and share your findings
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.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Things to consider when buying and using products.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to use an interrupted time series to evaluate your digital health product.
How to use feedback from marketplace reviews to evaluate your digital health product.
Why it's important to evaluate digital health products that have been developed rapidly and how to choose evaluation methods in these circumstances.
Information on OPSS product safety alerts, reports and recalls for unsafe products and resources for consumers, businesses and regulators.
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Use these general provisions to help you determine the origin of your products.
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
How the MHRA makes decisions on what is a medicinal product (borderline products).
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).