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 the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Guidance for the veterinary pharmaceutical industry on the production and submission of the Summary of Product Characteristics (SPCs) and product literature mock-ups.
Find out which radioactive sources you need a licence to export and how to apply for one.
Field inspection reports for the Genetic Modification Inspectorate deliberate release inspection programme in England.
You can use the PRE service to view recordings of pre-recorded evidence before trial.
Information about opinions requests we have received this year.
Check the tariff classification for preparations put up for retail sale.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Guidance on labelling for medicinal products used in clinical trials.
Guidance for Applicants wishing to apply for a Promising Innovative Medicines designation, pre-submission meeting or an EAMS Scientific Opinion.
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 and requires JavaScript).