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| Andrew C. von Eschenbach |
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Andrew C. von Eschenbach, M.D., is chairman of the Manhattan Institute's Project FDA. From September of 2005 to January 2009 he served as commissioner of the U.S. Food and Drug Administration where he championed an agenda to modernize the FDA. Dr. von Eschenbach joined FDA after serving for four years as director of the National Cancer Institute (NCI) at the National Institutes of Health where he set an ambitious goal to eliminate the suffering and death due to cancer by rapid acceleration and integration of the discovery-development-delivery continuum.
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| Dennis
A. Ausiello |
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Dennis
A. Ausiello, M.D., is the Jackson Professor of Clinical
Medicine at Harvard Medical School, and Chief of Medicine
at Massachusetts General Hospital (MGH). He is also a Director
of Pfizer, Inc. He has published numerous articles, book chapters,
and textbooks and served as the co-editor of Cecil's Textbook
of Medicine, in it's 22nd and 23rd. Dr. Ausiello is particularly
interested in the training of inquisitive physicians and translational
investigators, and is the architect and director of the Harvard
initiative in Patient-Associated Science: Training, Education,
Understanding, and Research (PASTEUR), a program designed
to introduce students to patient-oriented research and to
cultivate the development of the next generation of reflective
physician-scientists.
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| Arthur
Daemmrich |
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Arthur
Daemmrich, Ph.D., is an assistant professor in the Business,
Government, and the International Economy Unit at the Harvard
Business School and is a member of the interdisciplinary Harvard
Business School Healthcare Initiative. His work examines the
regulation of science-based industries, with an emphasis on
comparative risk analysis and the interplay of changing scientific
knowledge with business practices in the pharmaceutical and
chemical sectors. Dr. Daemmrich has published on pharmaceutical
regulation, biotechnology policy and politics, and innovation
in industrial chemistry.
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| Joseph
DiMasi |
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Joseph
DiMasi, Ph.D., is Director of Economic Analysis at the Tufts
Center for the Study of Drug Development at Tufts University.
His research is focused on the new drug development and regulatory
review processes and the economics of the pharmaceutical industry.
Dr. DiMasi presents his work at numerous professional and
industry conferences in the United States and abroad and has
testified before the U.S. Congress in hearings leading up
to the FDA Modernization Act of 1997 and reauthorization of
the Prescription Drug User Fee Act.
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| Henry
G. Grabowski |
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Henry
G. Grabowski, Ph.D., is a faculty member in the Health Sector
Management Program Faculty, a Professor of Economics and the
Director of the Program in Pharmaceuticals and Health Economics
at Duke University. Dr. Grabowski has published numerous studies
on the pharmaceutical industry with his principal research
involving the economics of the innovation process, business
regulation, industrial organization, and developing therapies
for Southern countries.
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| Paul
Howard |
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Paul
Howard, Ph.D., is a senior fellow and the director of the
Manhattan Institute's Center for Medical Progress. He is also
the managing editor of MedicalProgressToday.com, a web magazine
that chronicles the connections between market-oriented public
policies and better access to more innovative health care.
He focuses his research on a wide variety of medical policy
issues, including medical innovation, FDA reform, and consumer-driven
health care.
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| Daniel
P. Petrylak |
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Daniel
P. Petrylak, M.D., is an Associate Professor of Medicine and the Program Director of the Genitourinary Oncology Section in the Division of Hematology/Oncology at the Columbia University Medical Center. Dr. Petrylak has served on the program committee for the annual meetings of the American Urological Association (2003-7) as well as for the American Society of Clinical Oncology (1995-7, 2001-3). He also has served as a committee member for the Devices and Immunologicals section of the Food and Drug Administration Dr. Petrylak was instrumental in the clinical development of docetaxel for prostate cancer, and he chaired one of the trials that supported its approval for prostate cancer by the FDA in 2004. He was also one of the principal investigators on the SPARC trial, an international registration study of satraplatin, an oral chemotherapy agent, for patients who failed on chemotherapeutic regimen for prostate cancer
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| Tomas
J. Philipson |
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Tomas
J. Philipson, Ph.D., is a professor at the Harris School
for Public Policy at the University of Chicago. He is an associate
member of the Department of Economics and has been a Senior
Lecturer at the Law School. Dr. Philipson's research focus
is on health economics. He served in the Bush Administration
as the Senior Economic Advisor to the head of the Food and
Drug Administration (FDA) during 2003-04, as the Senior Economic
Advisor to the head of the Centers for Medicare and Medicaid
Services (CMS) in 2004-05 and is currently serving on an eight
member health care task force for Senator John McCain's campaign
for President of the United States.
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| Lance
K. Stell |
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Lance K. Stell, Ph.D., FACFE, is the John and Mary West Thatcher
Professor of Philosophy, Davidson College, Davidson, NC, where
he serves as Director of the Medical Humanities Program. He
also holds appointments as Clinical Professor in the Department
of Internal Medicine, at Carolinas Medical Center, Charlotte,
NC, and as Full Professor (Adjunct), in the Translational
Science Institute, at Wake Forest University School of Medicine,
Winston-Salem, NC. Dr. Stell is a Fellow and Diplomate
in the American College of Forensic Examiners. He consults
and serves as an expert witness in criminal and civil cases
in which the ethical standards of health care professionals
are implicated. He publishes in ethics, medical ethics and
philosophy of law. In 2005, the NC Medical Society recognized
Dr. Stell's service to the medical profession with the John
Huske Anderson award, the highest honor the Medical Society
bestows on a non-physician.
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| E. Fuller Torrey |
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E. Fuller Torrey MD is the Executive Director of the Stanley Medical Research Institute (SMRI) in Chevy Chase, Md. and the founder of the Treatment Advocacy Center in Arlington, VA. SMRI funds approximately 50 treatment trials at any given time for schizophrenia and bipolar disorder. Dr. Torrey was educated at Princeton, McGill and Stanford Universities and is the author of 20 books.
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