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Appendix C: Biographical Sketches of the Members and Staff of the Committee on the Use of Third Party Toxicity Research with Human Research Participants
Pages 173-184

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From page 173...
... Childress was Vice Chair of the national Task Force on Organ Transplantation, and he has also served on the Board of Directors of the United Network for Organ Sharing (UNOS) , the UNOS Ethics Committee, the Recombinant DNA Advisory Committee, the Human Gene Therapy Subcommittee, the Biomedical Ethics Advisory Committee, and several Data and Safety Monitoring Boards for National Institutes of Health Clinical Trials.
From page 174...
... At RFF, Taylor leads a research program on the policy and institutional issues affecting the success of the global food and agricultural system in areas such as food security in developing countries, food safety as a global concern, and the natural resource and environmental sustainability of agriculture. Publications include Redesigning Food Safety: Using Risk Analysis to Build a Better Food Safety System (2001)
From page 175...
... He has published more than 200 journal articles, book chapters, and abstracts. He has served on many National Academies Committees, including the Board on Environmental Studies and Toxicology Subcommittee on Acute Exposure Guideline Levels, the Committee on Health and Safety Consequences of Child Labor, the Committee on Pesticides in the Diets of Infants and Children, the Subcommittee on Dibromochloropane, and the Committee on Safe Drinking Water.
From page 176...
... Clayton has collaborated with faculty in the Law School, Medical School, and Sociology Department in producing interdisciplinary research. She has been an active participant in policy debates advising the National Human Genome Research Institute as well as numerous national and international bodies concerned with the ethical conduct of research involving humans for many years.
From page 177...
... He has received numerous awards from the Society of Toxicology, Robert Wood Johnson Medical School, International Society for Regulatory Toxicology and Pharmacology, Department of the Army, University of Chicago, American Conference of Governmental Industrial Hygienists, and American College of Toxicology. Doull currently serves on the National Academies Board on Environmental Studies and Toxicology and the Subcommittee on Acute Exposure Guidelines Levels.
From page 178...
... Higgins University Professor of Economics and Finance; Professor, Engineering and Public Policy, the H John Heinz III School of Public Policy and Management; Director, Green Design Initiative; and Co-director, Carnegie Mellon University Electricity Industry Center, Carnegie Mellon University.
From page 179...
... and the Data Safety Monitoring Board for NIHsponsored clinical trials in diabetes. Lo formerly was a member of the National Bioethics Advisory Commission and the Data Safety Monitoring Board for the AIDS Clinical Trials Group at NIH.
From page 180...
... Current applications include assessing the health effects of airborne particulate matter, assessing the cardio-pulmonary consequences of AIDS therapies, and reproductive health and the evaluation of teacher effectiveness. His Academy service includes membership on CNSTAT and on the Board of the Institute of Medicine's (IOM's)
From page 181...
... He has previously served on 16 Academy committees, including the Committee on Toxicological and Performance Aspects of Oxygenated Motor Vehicle Fuels, the Committee on Risk Assessment of Hazardous Air Pollutants, the Committee on Neurotoxicology and Models for Assessing Risk; the Committee on Human Health Risk Assessment of Using Antibiotics in Animal Feed, the Committee on Public Health Risk Assessment of Poultry Inspection, the Board on Toxicology and Environmental Health Hazards, the Subcommittee to Evaluate Effects of Short-Term Exposures to Drinking Water Contaminants (Chair) , and the Committee on Institutional Means for Assessment of Risks to Public Health.
From page 182...
... The Office of Medical Policy is responsible for regulation of promotion through the Division of Drug Marketing, Advertising, and Communication and for assessing quality of clinical trials and helping to assure participant protection through the Division of Scientific Investigations. Temple has a longstanding interest in the design and conduct of clinical trials and has written extensively on this subject, especially on choice of control group in clinical trials, evaluation of active control trials, trials to evaluate doseresponse, and trials using "enrichment" designs.
From page 183...
... He is a former Carl and Elizabeth Naumann Professor, Dean of Stanford University's School of Medicine, and Vice President of the University, as well as former Department of Pathology Professor and Chairman and Physician-in-Chief, Pathology, at Stanford University Hospital. He has served as the chair of the National Cancer Advisory Board (presidential appointment)
From page 184...
... Hanna, M.S., Ph.D., is a science and health policy consultant, writer, and editor in the Washington, D.C., area specializing in biomedical research policy and bioethics. She has served in senior staff and consulting positions with the National Bioethics Advisory Commission, the Presidential Advisory Committee on Gulf War Veterans Illnesses, the congressional Office of Technology Assessment, the Howard Hughes Medical Institute, the National Institutes of Health, and the Institute of Medicine.


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