Eric Chen serves as Director, Regulatory Affairs at Abbott. He assists with the management and leadership of regulatory activities with Abbott’s medical device business units, including the execution of strategic regulatory initiatives, regulatory filings, agency relationship and evaluation of regulatory policies. He also oversees the Medical Devices Regulatory Affairs Development Program that develops college graduates seeking a career in regulatory affairs by providing training and experiences with hands-on application in making life-saving products. Prior to Abbott, he had a 16-year career at FDA. He served as the Director of the Humanitarian Use Device (HUD) Program and Pediatric Device Consortia (PDC) Grants Program. He also served as an expert Biomedical Engineer responsible for the review and leadership of the mechanical circulatory support devices team.
Disclosure(s): Abbott Medical: Employee (Ongoing), Stockholder/Ownership Interest (excluding diversified mutual funds) (Ongoing)
Saturday, March 9, 2024
9:00 AM – 9:00 PM ET