We all try to be conscious of what we eat, so shouldn’t we be conscious of what medical devices are implanted in our bodies? Unfortunately, most people can’t make sense of the millions of adverse events filed with the FDA.
Today’s guest, Madris Kinard, left the FDA after years of seeing patients not get the data they need and started Device Events. Device Events is a subscription-based service that provides stakeholders with accessible information on products. Join Clay Hodges in this interview for more information on the gaps in the FDA, changes being made, and what Device Events does differently.