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 pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Advice for medical professionals to follow when assessing drivers with drug or alcohol misuse or dependence.
The MHRA has reviewed the latest evidence relating to the very rare risk of PRES and RCVS associated with medicines containing pseudoephedrine
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to prepare for implementation and compliance of the Safety Features Regulation.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Check what side effects people have reported when they've taken a medicine.
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
Guidance on medicines for food and non-food horses and record keeping requirements including the horse passport.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
The process for the simultaneous review of veterinary medicine submissions by New Zealand’s Ministry for Primary Industries (MPI) and the UK's Veterinary Medicines Directorate.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Guidance for prescribing vets on the use of the cascade.
Information and documents on Public Health England’s review of the evidence for dependence on, and withdrawal from, prescribed medicines.
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. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.