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
Systemic fluoroquinolones must now only be prescribed when other commonly recommended antibiotics are inappropriate. This follows a review by the MHRA which looked at the effectiveness of current measures to reduce the ident…
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
Marketing authorisations granted in 2024
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
The new presentation of Mounjaro gives four doses for once-a-week treatment over a month.
The MHRA will introduce a patient alert card to increase awareness among men taking finasteride about potential psychiatric and sexual side effects
Consumer advice and details of how to report problems with e-cigarettes with guidance on how to place an e-cigarette on the market in Great Britain and Northern Ireland, including the notification scheme.
Safety leaflet on topical corticosteroids and withdrawal reactions to help patients and their carers to use these medicines safely.
Submissions related to human medicines need to be submitted directly to the MHRA.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Guidelines for communicating clear and relevant information about machine learning-enabled medical devices.
Further detail on the arrangements giving effect to the Windsor Framework.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
MHRA services & information for patients and healthcare professionals.
Information on MHRA's enforcement duties and how to report a non-compliant medical device.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Manx Healthcare Ltd. has informed MHRA that they have identified a problem with the product packaging of the batch indicated in the table.
How to contact MHRA for specific services or enquiries.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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).