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 a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
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 to ensure the products you make or import comply with the law and are safe for consumers to use.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Check what you need to do to sell cosmetic products 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.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
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.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
How the MHRA makes decisions on what is a medicinal product (borderline products).
How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
Guidance for manufacturers, importers and distributors.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
When a material is waste, is a by-product or meets ‘end of waste’ status.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Guidance on prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
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.