New Tool Uncovers 10 Times More Adverse Events Than Regular Methods
This article was originally published in The Gray Sheet
Executive Summary
Two methods commonly used to track patient safety in hospitals fail to detect more than 90% of adverse events, according to a study of 795 hospitalized patients.
You may also be interested in...
MDRs Hit All-Time High, But FDA Still Says Adverse Events Are Underreported
FDA’s device center is concerned that adverse events are being grossly underreported to its Medical Device Reporting (MDR) program. This comes despite manufacturers submitting a record number of MDRs last year.
MDRs Hit All-Time High, But FDA Still Says Adverse Events Are Underreported
FDA’s device center is concerned that adverse events are being grossly underreported to its Medical Device Reporting (MDR) program. This comes despite manufacturers submitting a record number of MDRs last year.
Regulatory News In Brief
Sentinel workshop