Considerable proportion of medical device adverse events reported late
Although most manufacturer reports of medical device adverse events are reported on time, a considerable proportion are ...
STAT14h
Study reveals how often medical device makers report safety incidents late to FDA
Most medical devices in the United States come to market with limited clinical data, and device surveillance is viewed as a key way to keep patients safe. But the FDA’s system for collecting data and ...
MedTech Dive14h
EPA to reconsider emissions standards for medical device sterilizers
Last year, the EPA issued a final rule that would limit emissions of ethylene oxide, a cancer-causing gas used to sterilize ...