The Leading Forum on the Law, Regulation and Ethics of Medical Research in the United States

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The Leading Forum on the Law, Regulation and Ethics of Medical Research in the United States

THE 2ND ANNUAL MEDICAL RESEARCH SUMMIT

The Leading Forum on the Law, Regulation and Ethics of Medical Research in the United States

March 24 - 26, 2002
Grand Hyatt Hotel
Washington, DC



For future information about the Medical Research Summit and related educational events, please complete the form below.

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Featured Speakers:

William R. Braithwaite, MD, PhD
Director, PricewaterhouseCoopers, and former Senior Advisor on Health Information Policy, DHHS

Michael Carome, MD
Director, Compliance Oversight, Office for Human Research Protections, DHHS

Jeffrey M. Cohen, PhD
Associate Director of Education, Office for Human Research Protections, DHHS

Susan B. Ellenberg, PhD
Director, Office of Biostatistics and Epidemiology, Center for Biologics Evaluation and Research Food and Drug Administration, Rockville, MD

Alan E. Guttmacher, MD
Senior Clinical Advisor, National Human Genome Research Institute, NIH

David Hoffman, Esq.
Assistant U.S. Attorney, Civil Division, Eastern District of Pennsylvania

John Iglehart
Founding Editor, Health Affairs and National Correspondent, New England Journal of Medicine

Julie A. Kaneshiro
Office of Science Policy and Planning, NIH

Greg Koski, MD
Director, Office for Human Research Protections, DHHS

Richard Kusserow
President, Strategic Management Systems and former Inspector General, DHHS

Joanne R. Less, PhD
Director, IDE/HDE Programs, Center for Devices and Radiological Health, FDA

Mary Faith Marshall, PhD
Chairperson, National Human Research Protections Advisory Committee

John H. Mather, MD
Chief Officer, Office of Research Compliance and Assurance, Department of Veterans Affairs

Thomas Puglisi, PhD
Clinical Research Consulting Team, PricewaterhouseCoopers and Former Director, Human Subject Protections Office for Human Subjects Research Protections, DHHS

Michele Russell-Einhorn, Esq.
Director, Clinical Research Consulting Team, PricewaterhouseCoopers and Former Director of Regulatory Affairs Office for Human Research Protection

Sandra M. Sanford, RN, MSN, CCRC, CIP
Director of Human Research Protection Accreditation, NCQA

Karen Santoro, Esq.
Deputy Ethics Counselor, National Institute for Allergies and Infectious Diseases, NIH

Dixie R. Snider, Jr., MD
Associate Director of Science, CDC Marjorie A. Speers, Ph.D., Executive Director, Association for Accreditation of Human Research Protection Programs

Mark Yessian, PhD
Regional Inspector General for Evaluations and Inspections, Office of Inspector General, DHHS


Sponsored By:
Applied Clinical Trials
BNA's Health Care Program Compliance Guide
CenterWatch Monthly Newsletter
Clinical Trials Advisor
CW Weekly
Georgetown University Medical School
Harvard Health Policy Review
Health Affairs
Human Research Report
International Association of Privacy Officers
IRB Advisor
IRB Forum
IRB: Ethics & Human Research
Journal of Health Policy, Politics and Law
Medical Ethics Advisor
The Hastings Center Report
The Research Roundtable
Medical Education Collaborative
   A Nonprofit Education Organization


Educational Grantors:




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