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
Presentation given by Professor Sue Hill OBE, Chief Scientific Officer, England Download EMPEC presentation (PDF, 130K)
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
New report outlines the transformative potential of Engineering Biology to tackle modern-day challenges.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
How to conform with the legal requirements for placing medical devices on the market.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
Guidance on the importance of applying human factors to medical devices, so they are designed and optimised to minimise patient and user safety risks.
TechExpert is part of TechFirst, the government’s skills programme opening pathways into the UK’s fast-growing tech sector.
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 and requires JavaScript).