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Home : Info Center : Pike Article Zan Fleming Leaves Improved CDER Seminars as LegacyBy John Senior, MD G. Alexander "Zan" Fleming, MD, familiar to many as host of the weekly CDER Seminars for the past two academic years, has announced his plans to leave federal service at the end of August and to seek opportunities in private sector pharmaceutical research and development. He intends to remain based in the Washington area. Zan is a native of Nashville, Tenn., but grew up in Pensacola, Fla., the son of a busy practicing cardiologist who nevertheless found time to write and publish several books. He majored in biochemistry and molecular biology in college at Vanderbilt and the University of West Florida, followed by graduate work at Emory University before attending medical school there. He then trained in internal medicine and endocrinology, and subsequently was board-certified in both. It may be noted that he was elected president of both his college alumni and medical school classes. Zan was bitten by the research bug early in life and continued asking questions and seeking answers. As a medical staff fellow and senior staff fellow at the National Cancer Institute, he extended his early interests in the study of growth hormone effects on children to the investigation of amino acid derivatives as plasma signals for metabolic regulation. Zan joined CDER as a medical officer in the Division of Metabolic and Endocrine Drug Products in 1986 and three years later became a medical team leader in the division while continuing to see patients on a part-time basis. He was a primary medical reviewer for three important new molecular entities: lovastatin to treat high cholesterol and metformin and troglitazone to treat diabetes. For 18 months beginning in 1991, he was assigned to the World Health Organization in Geneva where he participated in writing the WHO good clinical practice document. Since its beginning in 1991, Zan has represented the FDA at International Conference on Harmonization meetings and is a member of the expert working groups on Good Clinical Practice (E-6) and on General Considerations for Clinical Trials (E-8). He has worked in China on drug development projects and in Russia, Ukraine and Belarus on accrediting FDA approvals in those countries. Zan is frequently asked to meet with foreign officials and scientists visiting the FDA. Most recently, he organized and participated in symposia on drug development and evaluation in Boston, Vienna, Moscow, Kuoshiung in Taiwan, Beijing, Seoul and London. In addition to becoming an excellent medical reviewer, Zan has continued to manifest outstanding vision, creativity and leadership. He has been an active contributor to the design and development of the CDER initiative on good review practices. Zan founded the Center's new virtual Journal and has served as its editor-in-chief. He wrote about initiating a career development path for medical reviewers, which came to fruition as the CDER Reviewer Career Path. As 1996-98 chair of the Committee for Advanced Scientific Education, he has fostered significant programmatic improvements in scientific excellence and a new atmosphere of collegiality at CDER Seminars. Zan has a special interest in the concept of task and problem focus in facilitating the drug development process. TPF is an issues-oriented means of communicating among drug developers and evaluators using an electronic, Web-like environment to capture organize, and store decisions and the data and other information on which they are based. TPF is being developed as a proof-of-concept project for the good review practices initiative. Some comments from his friends about this quintessential Renaissance man:
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