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.
FDA trade union: trade union: annual returns, rules, statement to members, decisions and other related documents.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Employment Appeal Tribunal judgment of Mrs Justice Eady on 20 May 2024.
Project Orbis is a programme to review and approve promising cancer drugs helping patients access treatments faster.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Information for patients, public and health care professionals.
Food and drink labelling and packaging regulations - what you must show, warnings, health and organic labels and packaging standards.
Members Statement for FDA
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
This document contains Other related Documents for FDA
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Rules for FDA.
A summary of recent letters and notifications sent to healthcare professionals about medicines and medical devices, and information about the publication of two recent Device Safety Information pages. The article also includes information on a recent National Patient Safety Alert...
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 MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
An MHRA and NICE partnership, funded by Wellcome, is addressing key challenges for regulating and evaluating digital mental health technologies (DMHTs) with input from patients, the public and mental health professionals.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised 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).