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
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.
How to use a behaviour change techniques review to evaluate your digital health product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Emerging Insights from DFID funded food markets programme in East and Southern Africa.
Things to consider when buying and using products.
CMA review indicates that some independent and smaller grocery retailers are failing to display clear and accurate prices.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
How to apply for simultaneous review of veterinary medicine submissions to the Australian Pesticides and Veterinary Medicines Authority (APVMA) and the VMD.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Procurement options available from the Crown Commercial Service for the public sector.
Find out when you can zero rate books and other forms of printed matter.
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.