Sr. Director, Regulatory Affairs
Sue has seventeen years in RA/QA at start-up, mid, and large-sized companies for a variety of medical devices, including implants, software, hardware, sutures, IVDs. She specializes in international strategy, registration, regulatory/cultural intelligence and quality systems.
Her training in cultural intelligence helped bridge the multi-cultural regulatory gaps at global companies and engage in harmonization efforts with the International Medical Device Regulators Forum (IMDRF).
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.
Tuesday, September 15, 2020
11:00 AM – 12:30 PM EDT