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Ten guiding principles that can inform the development of Good Machine Learning Practice (GMLP).
Guidance on the procurement of in vitro diagnostic (IVD) medical devices, their safety, quality and performance.
The Care Quality Commission (CQC) regulates all health and social care services in England. The commission ensures the quality and safety of care in hospitals, dentists, ambulances, and care homes, and the care given in people’s own homes. CQC is...
How to use a cost utility analysis to evaluate your digital health product.
How to conform with the legal requirements for placing medical devices on the market.
Guidance on the Quality Matters initiative, which aims to improve the quality of adult social care.
How to show MHRA you're meeting good clinical practice (GCP) standards and what to expect from an inspection.
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
A new framework for England that aims to raise quality in public health services and functions.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
The National Quality Board has published a final report setting out how quality will be maintained and improved in the new health system.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
This guidance outlines the scope and standards for medical physics services for the NHS breast screening programme.
A review of Defence Medical Services' compliance with the Care Quality Commission's essential standards for quality and safety in healthcare provision.
Government outlines action to make UK a world leader in tackling ethnic and other biases in medical devices.
How to register for the intensive care quality improvement programme (ICCQIP), a national intensive care unit infection surveillance programme in England.
An annual report which includes information on the performance of contractors and recognition of good practice.
A company director and his pharmaceutical manufacturing company were sentenced in court today after pleading guilty to two charges of falsifying data that supported the shelf life of a medicine, adversely affecting its quality in order to obtain a licence...
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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