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 apply for marketing authorisation via this new procedure.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
How to conform with the legal requirements for placing medical devices on the market.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
You may be able to get a one-off payment if you've been diagnosed with diffuse mesothelioma, and your exposure to asbestos happened in the UK
HM Revenue and Customs (HMRC) manages customers who deliberately don't pay taxes through the Managing Serious Defaulters (MSD) programme.
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
You must get permission to export certain drugs and medicines.
Government outlines action to make UK a world leader in tackling ethnic and other biases in medical devices.
Guidance for NHS regarding disclosure to individuals holding either a Lasting Power of Attorney or a deputyship.
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
How to use a combination of quantitative and qualitative data to evaluate your digital health product.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Find out about MCA's recruitment process for approved doctors (ADs).
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Advice for medical professionals to follow when assessing drivers with drug or alcohol misuse or dependence.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
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).