Between the recent publication of the "Implant Files" investigative reports, US FDA’s proposal to revise the 510(k) process to move away from the predicate model, and ongoing research into post-market patient safety, it’s clear media and government forces are devoting more attention to device safety. Medtech Insight spoke to two patient advocacy leaders about their efforts and future plans.
Amanda Dykeman and Holly Ennis both work with patient safety group ASHES Nonprofit, which grew out of the 20,000-member Facebook...
