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.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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 a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
The guide, toolkit and further information for GB authorities with responsibility for consumer product safety.
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.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Labelling rules for businesses in Great Britain (England, Scotland and Wales) and retailers in Northern Ireland, for certain agri-food products moved under the Northern Ireland Retail Movement Scheme.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
What animal by-products (ABPs) are, how to set up a site that uses them safely, the paperwork you need, and how to dispose of them.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Use these general provisions to help you determine the origin of your products.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Things to consider when buying and using products.
Guidance for suppliers and dealers.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
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).