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
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
All marketing and advertising must be: an accurate description of the…
Advertising to consumers The Consumer Protection from Unfair Trading…
There are 2 advertising codes of practice that describe how businesses…
You must describe your product accurately. This means if you make a claim…
You must check if customers want to be contacted by fax, phone, post or…
Submission dates and how the submissions using the EC decision reliance procedure work.
Explains control of advertisement regime.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
Form of advertisement of service by an alternative method (rule 6.15).
How the MHRA processes variations to Marketing Authorisations (MAs)
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to apply for marketing authorisation via this new procedure.
This strategy sets out Public Health England's 3-year strategic framework.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
This strategy sets out Public Health England's 3-year strategic framework and planned calendar of activity from 2014 to 2017.
Rules on labelling food, feed and seed as organic or using organic production terms if you produce, prepare, store, import, export or sell organic food in the UK.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical 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. 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.