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
Explains changes to drug driving law and the guidance available for healthcare professionals and users of prescription medicine.
NHS Business Services Authority contact number for ordering prepaid prescriptions for 3 or 12 months at a cheaper rate than single prescriptions
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
You must get permission to export certain drugs and medicines.
FCDO travel advice for USA. Includes safety and security, insurance, entry requirements and legal differences.
Guidance for healthcare and public health commissioners on planning treatment services for dependence on prescription and over-the-counter medicines.
Scope of the review of the evidence for dependence on, and withdrawal from, prescribed medicines.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Torrent Pharma (UK) Limited is recalling certain batches of Ramipril 1.25mg tablets as a precautionary measure due to these batches having a low assay and high related substances test results after their release to the market.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Check if someone selling medicines online in Northern Ireland is allowed to do so by the Medicines and Healthcare products Regulatory Agency (MHRA)
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
Information about new applications, post-licensing, advertising, product information and fees.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
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.