Kevin D. Bentley

Kevin D. Bentley has over 20 years of experience in regulatory affairs and quality management in the medical device industry. Kevin D. currently serves as the Vice President of Regulatory Affairs and Quality at ZOLL Medical Corporation, where they are responsible for regulatory strategy and compliance for new class III and class II products. Prior to this, Bentley was the Company Owner of Acumen Regulatory and Quality Consultants, where they provided global medical device registration assistance and developed electronic quality management systems for medical device companies. Kevin D. also served as the Executive Director of Regulatory Affairs and Quality at LSI Solutions, where they led the regulatory, quality, and corporate training departments. Bentley has experience with FDA regulatory pathways, international clinical studies, and corporate integration. Before that, they held positions as the Director of Regulatory Affairs and Quality Assurance at Angel Medical Systems and Angiotech, and as the Director of Quality and Regulatory Affairs at STS Biopolymers.

Kevin D. Bentley attended Rochester Institute of Technology, where they studied Chemistry with a focus on Polymer Chemistry and Quality. Kevin D. then pursued Master's degree coursework at Northeastern University, with a concentration in Regulatory Affairs. In addition to their education, Kevin also holds a certification in Regulatory Affairs (RAC).