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 on granted EAMS scientific opinions, including the public assessment report and treatment protocols.
Industry must notify the MHRA if they will not be using these flexibilities
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Manufacturer licences including importer licences, specials, investigational and non orthodox and wholesale distribution licences.
Letter about the importance of handling and storing medicines in a safe and secure manner
Medicines that were granted a positive opinion under the early access to medicines scheme (EAMS) which has now expired.
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
Qualified Persons (QPs) should follow the below guidance on the flexible approaches we are taking for medicines imported from third countries.
Actions that trial sponsors should consider to build resilience into clinical trial design
Guidance following recommendations from the Commission on Human Medicines.
Guidance to help medicine manufacturers meet safe limits on levels of nitrosamine impurities in medicines.
The legal text underpinning the regulation of manufacture, authorisation, marketing, distribution, use and post-authorisation surveillance of veterinary medicines and medicated feed.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Guidance on how to reclassify your medicine and how to name medicines.
Cygnus Pharma Ltd. Have informed MHRA that the European Article Number (EAN) barcode printed on various packs of Trazodone Hydrochloride 50mg/5ml Oral Solution, is defective and returns the incorrect information.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
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).