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 to label spirit drinks that you plan to sell in the UK.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Apply to export or move poultry meat from Great Britain to the EU or Northern Ireland.
How to submit your periodic safety update report report (PSUR) or periodic benefit risk evaluation report (PBRER)
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Find out about applying for the Spirit Drinks Verification Scheme, how to submit brand information, fees and making sure your production process is compliant.
Find out about the UK geographical indication (GI) schemes that protect the geographical names of food, drink and agricultural products, and the UK GI schemes registers.
Guidelines on the acceptance of pleas and the prosecutor's role in the sentencing exercise (revised 2009).
You must batch and label the beef and veal you sell or supply according to specific rules, which vary from product to product.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
Information about the EU Regulations and their implementation in Northern Ireland
Guidance for service users on the approved indications for polio serological testing.
Seeking views on proposed changes to GI schemes (including the protected food name scheme) to bring these into UK law after Brexit.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Apply for protection against infringements of intellectual property rights on imports into and exports out of the UK.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
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.