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Ten guiding principles that can inform the development of Good Machine Learning Practice (GMLP).
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Millions invested in eight innovative companies behind lifesaving new medical technology which could destroy liver cancer tumours, detect Alzheimer’s and quickly spot those at risk of stroke
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Government outlines action to make UK a world leader in tackling ethnic and other biases in medical devices.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to use a cost utility analysis to evaluate your digital health product.
Advice and guidance on the health needs of migrant patients for healthcare practitioners.
The government’s plan to support a thriving UK medtech sector and make sure the health and care system can reliably access safe, effective and innovative medical technologies to deliver the best outcomes for patients.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Guidance on the Quality Matters initiative, which aims to improve the quality of adult social care.
Achievements made since the launch of the medtech strategy and the next steps to boost the adoption of medical technology in the NHS.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Information and guidance on a range of medical devices for users and patients.
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