*This is an archive page. The links are no longer being updated. 1993.02.03 : Appointment -- Bruce Burlington Contact: Betsy Adams - (301) 443-4177 (Home) - (410) 867-0679 February 3, 1993 Commissioner of Food and Drugs David A. Kessler, M.D., today announced the appointment of Bruce Burlington, M.D., as director of the Food and Drug Administration's Center for Devices and Radiological Health. The center is responsible for ensuring the safety and effectiveness of all medical devices, including heart valves, breast implants, hip and joint replacements and hospital equipment. The center also ensures the safety of consumer and medical radiation-emitting equipment, such as x-ray machines, microwave ovens, mammography machines and television sets. "Dr. Burlington has demonstrated his ability to resolve complex issues of health and public policy, and he is a strong and effective manager," Dr. Kessler said. "His experience in enhancing product development and review across the agency -- in biologics, in generic drugs and, most recently, with new drugs -- will serve him well in the regulation of new medical technologies. "These technologies can mean the difference between life and death," Dr. Kessler added, "and Dr. Burlington's appointment demonstrates FDA's commitment to fostering the availability of safe and effective medical devices." Dr. Burlington joined FDA in 1981. Since 1988, he has been director of the Office of Drug Evaluation II in the Center for Drug Evaluation and Research (CDER), with responsibility for scientific and managerial supervision of anti-infective, antiviral, metabolic and endocrine drug products. From 1989 to 1990, he also served as acting director of the Office of Generic Drugs. Since 1990, he has held the post of deputy director for medical affairs of CDER, as a collateral duty. "In his medical affairs post, Dr. Burlington has been especially active in international harmonization of drug approval standards, program accountability and productivity," said Deputy Commissioner for Operations Jane E. Henney, M.D. "He has been particularly effective in dealing with complex issues related to the planning and implementation of user fees as well as the effective use of the agency's scientific advisory committees." From 1986 to 1988, Dr. Burlington was in charge of the division of biological investigative new drugs in the Center for Biologics Evaluation and Research. And, from 1981 to 1986, he was a research fellow and then chief of the respiratory virus laboratory in FDA's biologics unit. Dr. Burlington earned his medical degree from Louisiana State University School of Medicine in 1975. He came to FDA after completing his internship and residency in medicine and a University of Colorado Medical Center. He succeeds James S. Benson, who recently left the government after a long and distinguished career in federal service. The FDA is one of eight Public Health Service agencies in HHS. ###