Summary
An ideal surveillance system for medical device safety would comprehensively collect data on adverse events across the life span of a device, discusses Salazar and Redberg in an Editorial in JAMA Internal Medicine. They suggest that the system should be integrated into electronic health records to allow seamless identification, tracking, and real-time reporting of device-associated adverse events. It would be able to take adverse events and detect substantial safety signals and underperforming devices. Such a system would also allow implementation of corrective actions quickly.
JAMA: Editorial. Leading the call for reform of medical device safety surveillance
https://jamanetwork.com/journals/jamainternalmedicine/fullarticle/2757526?resultClick=1
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