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
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Check what UIDs you need for your tobacco products and the specifications they need to meet.
How to prepare for implementation and compliance of the Safety Features Regulation.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to apply to protect a food, drink or agricultural product name under the UK GI schemes.
What intellectual property is, how you can protect it, and which of copyright, patents, design right and trade marks applies to your work
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
Use these general provisions to help you determine the origin of your 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.
Find out if you will need to use the new UKNI marking and how to use it.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
Use the case studies to help you decide when your goods may (or may not) go beyond insufficient production.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
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.
Check what processes are considered as insufficient production under the Trade and Cooperation Agreement.
Find out what compound products are, and how to import or move them from the EU to Great Britain.
How product specific rules are used to identify the country of origin when importing or exporting between the UK and EU.
Find out the rules to establish the country of origin of imported and exported goods and to help identify goods which qualify for lower or no Customs Duty.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
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).