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Suggested Citation:"Appendix B: Speakers and Panelists." Institute of Medicine. 1999. Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making: Workshop Report. Washington, DC: The National Academies Press. doi: 10.17226/9623.
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Appendix B
Speakers and Panelists

Susan Alpert, M.D., Ph.D.

Director of Device Evaluation

Center for Devices and Radiological Health

Food and Drug Administration

Robert Califf, M.D.

Director

Duke Clinical Research Institute

Michaele C. Christian, M.D.

Associate Director, Cancer Therapy Evaluation Program

Division of Cancer Treatment

National Cancer Institute

Michael Clayman, M.D.

Vice President

Cardiovascular Research and Clinical Investigations

Lilly Research Laboratories

Eli Lilly and Company

Susan Ellenberg, Ph.D.

Director

Division of Biostatistics and Epidemiolgy

Center for Biologics Evaluation and Research

Food and Drug Administration

Ronald Estabrook, Ph.D.

Professor of Biochemistry

University of Texas

Southwestern Medical Center

William Fairweather, Ph.D.

Associate Director

Office of Epidemiology and Biostatistics

Food and Drug Administration

Frank L. Hurley, Ph.D.

Chief Science Officer

Quintiles Transnational Corporation

Suggested Citation:"Appendix B: Speakers and Panelists." Institute of Medicine. 1999. Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making: Workshop Report. Washington, DC: The National Academies Press. doi: 10.17226/9623.
×

Charma Konnor

Director

Bioresearch Monitoring Division

Office of Compliance

Center for Devices and Radiological Health

Food and Drug Administration

Kiyoshi Kuromiya

Critical Path AIDS Project

David Lepay, M.D., Ph.D.

Director

Division of Scientific Investigations

Food and Drug Administration

Robert Levy, M.D.

Senior Vice President, Science and Technology

American Home Products

Wyeth-Ayerst Research

Murray Lumpkin M.D.

Deputy Director for Review Management

Center for Drug Evaluation and Research

Food and Drug Administration

Michael McGarvey, M.D.

Chief Medical Officer

Blue Cross and Blue Shield of New Jersey, Inc.

Roger Meyer, M.D.

Senior Consultant

Division of Biomedical and Health Sciences Research

American Association of Medical Colleges

Kristin O'Connor, M.P.H.

Director, Data Management

Boehringer Ingleheim Pharmaceuticals, Inc.

Nicholas Pelliccione, Ph.D.

Senior Director

Worldwide Regulatory Affairs

Schering Plough

Jim Phillips, Ph.D.

Senior Director for Biostatistics

Quintiles Transnational Corp.

John Schultz, Ph.D.

Vice President

General Manager

Neuroclinical Trials Center

University of Virginia

Eleanor Segal, M.D.

Senior Director

Drug Safety and Clinical Quality Assurance

Chiron Corporation

Kenneth I. Shine, M.D.

President

Institute of Medicine

Jay Siegel, M.D.

Director

Office of Therapeutics Research and Review

Center for Biologics Evaluation and Research

Food and Drug Administration

Whaijen Soo, M.D., Ph.D.

Vice President, Clinical Sciences

Roche Pharmaceuticals

Hoffmann-La Roche, Inc.

Frances Visco, J.D.

President

National Breast Cancer Coalition

Suggested Citation:"Appendix B: Speakers and Panelists." Institute of Medicine. 1999. Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making: Workshop Report. Washington, DC: The National Academies Press. doi: 10.17226/9623.
×

William Waggoner, Ph.D., FAACT

Chairman

Essex Institutional Review Board, Inc.

Janet Woodcock, M.D.

Director

Center for Drug Evaluation and Research

Food and Drug Administration

Stan Woollen

Deputy Director

Division of Scientific Investigations

Center for Drug Evaluation and Research

Food and Drug Administration

Suggested Citation:"Appendix B: Speakers and Panelists." Institute of Medicine. 1999. Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making: Workshop Report. Washington, DC: The National Academies Press. doi: 10.17226/9623.
×
Page 56
Suggested Citation:"Appendix B: Speakers and Panelists." Institute of Medicine. 1999. Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making: Workshop Report. Washington, DC: The National Academies Press. doi: 10.17226/9623.
×
Page 57
Suggested Citation:"Appendix B: Speakers and Panelists." Institute of Medicine. 1999. Assuring Data Quality and Validity in Clinical Trials for Regulatory Decision Making: Workshop Report. Washington, DC: The National Academies Press. doi: 10.17226/9623.
×
Page 58
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In an effort to increase knowledge and understanding of the process of assuring data quality and validity in clinical trials, the IOM hosted a workshop to open a dialogue on the process to identify and discuss issues of mutual concern among industry, regulators, payers, and consumers. The presenters and panelists together developed strategies that could be used to address the issues that were identified. This IOM report of the workshop summarizes the present status and highlights possible strategies for making improvements to the education of interested and affected parties as well as facilitating future planning.

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