In May, a manufacturer of a non-OEM AED replacement battery received a Warning Letter from the FDA, following an inspection that occurred last November. Here, educator William Hyman breaks down the implications this could have for the industry.
In this installment of CE Reflections, Rick Schrenker, a systems engineering manager for Massachusetts General Hospital and industry veteran, discusses the normalization of deviance—and how it applies to HTM departments.
Winners of this year’s competition were awarded up to $25K each at the Children's National Sixth Annual Pediatric Device Innovation Symposium, held in Philadelphia on September 23. This year’s competition focused on pediatric cardiovascular devices, an area of significant need where advancements can make life-saving differences in the care of children.