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
Following MHRA approval of a clinical trial, a study on Nuwiq, a recombinant FVIII therapy for the treatment of haemophilia A, can proceed.
Find out about MCA's recruitment process for approved doctors (ADs).
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
Submissions related to human medicines need to be submitted directly to the MHRA.
Information on how to apply for jobs, workplace benefits and skills development at the Agency.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Information for British citizens moving to or living in Liberia, including guidance on security, healthcare and driving.
Guidance for industry on flexible approaches we are taking on good distribution practices.
Advice for medical professionals to follow when assessing drivers with drug or alcohol misuse or dependence.
Guidance on the 150-day assessment timeline for high-quality marketing authorisation applications including information on how to apply.
Information for British people on medical support in Thailand including mental health, lists of hospitals and care homes and how the British embassy can help.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
The Work and Health Programme helps you find and keep a job if you're out of work - eligibility, how to claim.
Veterinary Pharmacovigilance Assessor vacancy, working in the regulation of veterinary medicines.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Employers might monitor workers, but if the monitoring involves taking data, images or drug testing they have to do this in a way that's legal and fair
The CMU is part of the Medicine, Pharmacy and Industry Group of DHSC which looks at supply and procurement in hospitals.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
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).