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.
Information for wholesale dealer licence holders about the medicines put on the UK market for UK patients that they cannot export or hoard.
How to apply for marketing authorisation via this new procedure.
Information about controlled drugs licences for companies that possess, manufacture, produce or supply controlled drugs in England, Wales or Scotland.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Check what side effects people have reported when they've taken a medicine.
Anyone in Northern Ireland selling medicines to the public via a website must still comply with the requirement to apply the EU common logo.
Neon Healthcare Ltd is recalling the specific batch mentioned in this notification as a precautionary measure.
Guide to submitting research applications to the Administration of Radioactive Substances Advisory Committee (ARSAC).
How to prepare for implementation and compliance of the Safety Features Regulation.
How to change the ownership from one marketing authorisation (MA) holder to another.
How veterinary medicines can be advertised.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
Pharmacovigilance system requirements
Information about new applications, post-licensing, advertising, product information and fees.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Jan - 31 Mar 2024.
The legal text underpinning the regulation of manufacture, authorisation, marketing, distribution, use and post-authorisation surveillance of veterinary medicines and medicated feed.
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).