Microtest Laboratories has issued a management brief that discusses reusable medical device cleaning validation and testing practices in view of the FDA’s own discussions and actions around ...
Facility & Process Validation is a component of the quality assurance framework of pharmaceutical, biotechnology, and medical device manufacturing. It is a process used to evaluate the manufacturing ...
Health care leaders may want to keep a closer eye on clinical validation for artificial intelligence (AI)-enabled medical devices (AIMDs), based on a recent JAMA Health Forum study.
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