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| WELCOME AND OPENING REMARKS |
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Kathryn M. Carbone
M.D., Science Forum Organizing Committee
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Norris E. Alderson
Ph.D., Associate Commissioner for Science
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Mark B. McClellan, M.D., Ph.D.
Commissioner of Food and Drugs
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Keith Carson
Williamsburg BioProcessing Foundation
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| OPENING ADDRESS |
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HHS Initiatives that Protect America’s Health Tommy Thompson
Secretary, Department of Health and Human Services
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| KEYNOTE ADDRESS |
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Lessons from Swine Flu in an Age of Bioterrorism Harvey V. Fineberg, M.D. Ph.D.
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| Science: The Cornerstone of Risk Assessment and Management |
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Enhancing the Role of Science in Stakeholder-Based Risk Management Decision-Making Gail Charnley, Ph.D.
Health Risk Strategies
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Introduction to Bioinformatics Dan Casciano
Ph.D., National Center for Toxicological Research, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Microbial and Antimicrobial Resistance Risk Analysis: Emerging Hazards Meet Re-Emerging Science H. Gregg Claycamp, Ph.D.
Center for Veterinary Medicine (No relationships, financial or otherwise, to disclose in relation to this presentation)
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FDA Science: Ahead of the Curve Chaired by Norris E. Alderson, Ph.D., Associate Commissioner for Science |
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Bacterial Evolution, Mutators, and the Emergence of Pathogens Tom Cebula, Ph.D.
Center for Food Safety and Applied Nutrition, FDA
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Cancer, Apoptosis, and Oxidative Stress: What's Protein S Got To Do With It? Emily Shacter, Ph.D.
Center for Biologics Evaluation and Research, FDA
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Forensic Investigation Related to Food and Pharmaceutical Tampering and Counterfeiting S. Frank Platek, M.S.
Office of Regulatory Affairs, FDA (Includes discussion of a commercial product however he claims no interest, financial or otherwise, in the manufacturer and he will discuss case-related items/products involving tampering and/or counterfeiting of food, beverage and pharmaceutical products.)
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Public Health Initiatives in the Aftermath of 9/11 Chaired by |
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NIH Perspectives Elias Zerhouni, M.D.
National Institutes of Health
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Did Events of 9/11 and Later Make Us A Better FDA? Bernard A. Schwetz, D.V.M., Ph.D.
FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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National Level Priorities and Preparedness David W. Fleming, M.D.
Centers for Disease Control and Prevention D.V.M
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New Technologies for Assessing and Predicting Risk: Application of Bioinformatics Chaired by |
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Development of a Toxicoinformatics Integrated System at NCTR Weida Tong, Ph.D.
National Center for Toxicological Research, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Serum Proteomic Pattern Diagnostics Using Artificial Intelligence Based Bioinformatics Emanuel F.Petricoin, Ph.D.
Center for Biologics Evaluation and Research, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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An Integration of Genomic, Proteomic, and Metabonomic ApproachesTo Better Evaluate Drug-Associated Cardiovascular Risks Frank D. Sistare, Ph.D.
Center for Drug Evaluation and Research, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Incorporation of Toxicogenomics into Mechanistic and Predictive Toxicology: Analysis of the Effects of Ethynyl Estradiol on Uterine Gene Expression Timothy Zacharewski, Ph.D.
Michigan State University
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Defining Cancer Risk Chaired by |
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Thresholds, Risk Assessment, and Setting the Limits of Regulation Mitchell A. Cheeseman, Ph.D.
Center for Food Safety and Applied Nutrition, FDA
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Using Computational Toxicology to Screen Chemicals for Carcinogenic Potential Joseph F. Contrera, Ph.D.
Center for Drug Evaluation and Research, FDA
(Includes discussion of commercial product, and presenter has a CRADA with Multicose, Inc. and otherwise claims no relationships, financial or otherwise, to disclose in relation to this presentation.)
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Relevance of Model Somatic Mutation Systems for Humans Richard J. Albertini, Ph.D
University of Vermont
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Unified Approach for Cancer and Non-cancer Risk Assessment Ralph Kodell, Ph.D.
National Center for Toxicological Research, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Host Responses to Medical Interventions Chaired by |
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Protective Innate Immune Responses Elicited by CpG Oligonucleotides Dennis Klinman, M.D., Ph.D.
Center for Biologics Evaluation and Research, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Replacement Heart Valve-Related Pathology: In Vivo Preclinical Studies Stephen L. Hilbert, M.D., Ph.D.
Center for Devices and Radiological Health, FDA
(Includes discussion of a commercial product however he claims no interest, financial or otherwise, with the manufacturer and off-label use will not be discussed.)
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PET Imaging and Pharmacokinetics Jerry Collins, Ph.D.
Center for Drug Evaluation and Research, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Cancer : Origins, Diagnosis, Treatment and Prevention Chaired by |
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Cytokine Receptors as Targets of Cancer Therapy Raj K. Puri, M.D., Ph.D.
Center for Biologics Evaluation and Research, FDA
(Includes discussion of unlabeled/investigational use of a commercial product in presentation therapeutic targeted agent discovered at CBER, and has CRADA with NeoPharm, Inc., and otherwise claims no relationships, financial or otherwise, to disclose in relation to this presentation.)
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Cancer Susceptibility, Early Detection Luke Ratnasinghe, Ph.D., M.P.H.
National Center for Toxicological Research, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Effects of Exposure to Estrogens at Various Life Stages on Reproductive Endpoints and Cancer K. Barry Delclos, Ph.D.
National Center for Toxicological Research, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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Diagnostic Imaging, Reader Variability, Computer Aids – and the Quest for the Holy Grail Robert F. Wagner, Ph.D.
Center for Devices and Radiological Health, FDA
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On the Scene: Detecting Biological and Security Risks Chaired by |
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Collaborative Efforts to Promote Diagnostic Platform Development Maj. Wilson, Ph.D.
Department of Defense
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Development of Real-Time PCR Tests for Agents Causing Smallpox and Anthrax Thomas F. Smith, Ph.D.
Mayo Clinic and Foundation
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FDA’s Role in Security Screening Systems: Radiation Risks, Privacy Laws, and Public Concern Orhan Suleiman, Ph.D.
Office of the Commissioner, FDA
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Emerging Issues in Risk Communication Chaired by |
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Public Participation in Risk Communication Ned Groth III, Ph.D.
Consumers Union
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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When Science and Society Conflict: A Diagnostic Model for Risk Communication Stephen F. Sundlof, D.V.M., Ph.D.
Center for Veterinary Medicine, FDA
(No relationships, financial or otherwise, to disclose in relation to this presentation)
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FDA and the Media: Communicating Risk to the Public Lauran Neergaard
Associated Press
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Internet2 Workshop Chaired by |
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Introduction Mary Kratz, M.T.(A.S.C.P.)
Internet2 Health Sciences
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The Next Generation Internet, Internet2 & the National Library of Medicine Paul Fontelo, MD, MPH
Office of High Performance Computing and Communications
National Library of Medicine
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The Future of Health and Internet2 of the Future
Victor Frankel, M.D.
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Clinical Realities David J. Polly, Jr., M.D.
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