Sue has more than fifteen years in Regulatory Affairs and Quality Assurance at start-up, mid and large-sized companies for a variety of medical devices including implants, software, hardware, sutures and IVDs. She specializes in global strategy, registration, regulatory/cultural intelligence and quality systems. Sue has her RAC through the Regulatory Affairs Professionals Society (RAPS) and MS in Regulatory Affairs. She also completed the Kellogg Executive Leadership Program at Northwestern University.