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.
How to use an ethnographic study to evaluate your digital health product.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
Comply with good pharmacovigilance practice and prepare for an inspection.
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.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Find out when it's possible to get zero-rated supplies on medical and research goods and services that have been funded by charities.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Chief Medical Officer for England, Professor Chris Whitty's annual reports and lectures on medicine and public health.
Medical advisory panels work with DVLA to provide expert advice, with the aim of improving road safety. See information on their role and current vacancies.
Checklists providing a practical guide to using medical devices.
Legal requirements and good practice guidance for Veterinary Practice Premises Inspections.
How to use a cost utility analysis to evaluate your digital health product.
The Medical Profession brings together doctors from across the Civil Service. Medical Profession is part of the Civil Service .
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).