Ximedica Offers Usability Expertise As Conferees at MD&M-West Ponder FDA’s New Emphasis on Human Factors in Medical Devices Posed by HE-75

PROVIDENCE, R.I.--(BUSINESS WIRE)--As medical device industry professionals convene at MD&M-West this week, speed to market and its necessary corollary, FDA approval, are foremost on the agenda. Of special interest will be the new HE-75 practice guidelines, which were established by ANSI/AAMI and endorsed by the Food and Drug Administration.