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Products > Health Care Compliance Association > HCCA’s 2007 ANNUAL COMPLIANCE INSTITUTE
308: Advantages of a Comprehensive Adverse Event Reporting System

SPEAKER: Joan Caron, Director, Office of Research Compliance; Assistant Professor, Department of Cell Biology, University of Connecticut Health Center

  • Ethical treatment of human subjects
  • A novel comprehensive compliance monitoring program for adverse event reporting in clinical trials
  • Keeping human subjects safe during clinical trials

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