Sue Hibbeln, MS, RAC

VP
Lumos Diagnostics

Sue Hibbeln has more than 20 years industry experience in Regulatory Affairs and Quality Assurance at start-up, mid- and large-sized companies for a variety of medical devices, including in vitro diagnostic devices, software, hardware, implants and sutures. Sue is a CMMI Practitioner and a certified appraisal team member (ATM) for the Medical Device Discovery Appraisal Program (MDDAP), part of FDA's VIP (Voluntary Improvement Program).

She also currently serves as Vice President of Quality and Regulatory Affairs for Lumos Diagnostics, Inc. where she specializes in global strategy, registration, regulatory/cultural intelligence and quality systems.

Presentation(s):

• Sharpening Your Regulatory Soft Skills Toolbox

  Monday, September 16, 2024
  8:30 AM – 4:00 PM PDT