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
Check what you need to do to sell cosmetic products in Great Britain.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
What you need to know about and do to comply with the law and keep consumers safe.
Things to consider when buying and using products.
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.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
How to create a model of how your digital health product works and choose measures for your evaluation.
How you import from and export to Turkey.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
The rules about product labelling - including special rules for retailers and manufacturers in different business sectors (like food, jewellery and toys)
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
Guidance for manufacturers, importers and distributors.
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. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.