Shannon Bennett, MS, MBA, is a seasoned professional with more than two decades of experience in the clinical diagnostics field. Currently serving as the director of regulatory affairs in the Department of Laboratory Medicine and Pathology at Mayo Clinic, Bennett brings a wealth of expertise to the intersection of health care and regulatory compliance. He holds a master’s degree in biochemistry and structural biology, complemented by an MBA. Additionally, Bennett is a certified manager of quality and organizational excellence through the American Society for Quality, showcasing a commitment to the highest standards in the field. Throughout his career, Bennett has been a driving force influencing requirements for the design, development, and validation of laboratory-developed tests (LDTs). He is dedicated to sharing insights, fostering innovation, and contributing to the continual improvement of diagnostic testing.
Articles by Shannon Bennett, MS, MBA
Navigating FDA’s LDT Final Rule: Key Terminology Every Clinical Lab Should Know
As the first milestone of the new LDT Final Rule approaches, here are the key FDA terms laboratories need to understand
