The Impact of COVID-19 on Medical Device Reporting and Investigation [0.03%]
新冠肺炎疫情对医疗器械不良事件报告和监测的影响
Zoe Pruitt,Christian Boxley,Seth A Krevat et al.
Zoe Pruitt et al.
Introduction: The Manufacturer and User Facility Device Experience (MAUDE) database houses medical device reports submitted to the U.S. Food and Drug Administration (FDA). In May 2020, the FDA released guidance about medi...