Dr. Brenner serves in the Office of In Vitro Diagnostics in the Center for Devices and Radiological Health as a principal advisor to the Office Director, Center Director, and other key officials on regulatory premarket and post-market compliance and surveillance issues, with influence on Center and Agency level decisions, policy development nationwide, program execution, and progression of short and long range program goals and objectives. She provides leadership and scientific direction to a multidisciplinary medical, scientific, and professional staff engaged in developing and implementing standards for the safety and effectiveness of medical devices marketed and used throughout the United States.