Read the full report in Becker’s ASC Review on medical device-related adverse events.
230,000 Medical Device Adverse Events Reported to FDA in 2010
Of the more than 230,000 medical device-related adverse events reported to the Food and Drug Administration in 2010, approximately 30,000 yielded “very serious” outcomes such as hospitalization or death, according to research conducted by Clarimed.
From concept to impact: Standing up an office of well-being
Presenters: Jim Gilligan, American Medical AssociationEve Poczatek, MBA, SPHR, Rush University System for Health
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