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
Guidance for holders of Marketing Authorisations approved in Northern Ireland or the EU/EEA member states who want to bring a product to market in Great Britain.
Confirmation of the regulation 251 of the Human Medicines Regulation following the Brexit transition.
A set of principles for understanding the impact of new variants on antiviral drugs and monoclonal antibodies
A letter providing guidance on the post-transition conversion process was sent by email on 23 October 2020 to the Community MA holders.
MHRA scientific and regulatory advice for COVID-19 vaccine developers
If pharmacies wish to ‘pack down’ larger packs of a medicinal product, they need to follow these instructions
Update about the developing role of biosimilar medicines in the NHS in England and the safe, effective and consistent use of biosimilar medicines.
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).