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.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
Guidance for UK companies on winning business from international aid and development projects.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance for the veterinary pharmaceutical industry on how to apply for and maintain a shared-label for use on veterinary medicines placed on the market in the UK and Ireland.
Use this form to transfer a product licence, also known as a marketing authorisation, to a different owner.
Pharmacovigilance system requirements
Guidance for manufacturers, importers and distributors.
How to transfer the ownership of a marketing authorisation including the form you need to complete.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How veterinary medicines can be advertised.
How to market forest reproductive material (FRM) for forestry purposes, including regulations, registration, master certificates and licences.
Find out what makes a person an enabler of tax avoidance, and what to do about legally privileged communications.
Information for people who wish to apply to release a vaccine or a blood product to market in the UK.
Processes for marketing authorisations granted before 31 December 2020, or submitted or ongoing from 1 January 2021.
The European Union (EU) and European Economic Area (EEA) - which countries are in the EU and EEA, the single market and free movement of goods, capital, services and people
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Find out the rules from 1 January 2018 if you promote or use arrangements that are meant to give someone a VAT or other indirect tax saving or a tax deferral.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
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).