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 the MHRA makes decisions on what is a medicinal product (borderline products).
How to create a model of how your digital health product works and choose measures for your evaluation.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
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 the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
Use a separate statement of objection form for each Moldovan geographical indication (GI) product name you object to.
Things to consider when buying and using products.
What you need to know about and do to comply with the law and keep consumers safe.
Ensuring you get what you pay for.
How to apply for UK protection of a traditional term for a wine product and get it added to the UK traditional terms register.
Papers from the Office for Product Safety and Standards.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
Use a separate statement of objection form for each Georgian GI product name you object to.
Find out which regulations apply to your products and where to go for further information on how to comply with them.
The UK’s consumer connectable product security regime came into effect on 29 April 2024. Businesses in the supply chains of these products now need to be compliant with the legislation.
Our primary purpose is to protect people and places from product-related harm, ensuring consumers and businesses can buy and sell products with confidence. Office for Product Safety and Standards is part of the Department for Business and Trade .
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
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).