ATLANTA — For years medical device makers have fired off concerns and criticisms of the FDA's regulatory process – at times going so far as to call it unpredictable. Last week, during the Southeastern Medical Device Association's (SEMDA; Norcross, Georgia) annual conference held at the Georgia Institute of Technology Global Learning Center (Atlanta), med-tech firms got the chance to hear directly from the Center for Devices and Radiological Health's (CDRH) director – Jeffrey Shuren. Read More
