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Conflicts, Compliance, and Enforcement: Government Priorities and Initiatives

Fraud, conflict of interest, and other enforcement issues in clinical research

Guy M. Chisolm, PhD and James G. Sheehan
Cleveland Clinic Journal of Medicine March 2007, 74 (3 suppl 2) S63-S67;
Guy M. Chisolm III
Vice Chairman, Lerner Research Institute, Professor, Department of Cell Biology Cleveland Clinic
Roles: Supplement Editor
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James G. Sheehan
Associate US Attorney, US Attorney’s Office, US Department of Justice, Philadelphia, PA
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  • For correspondence: [email protected]
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ABSTRACT

Fraud in scientific research is a widespread problem. It can involve falsifying data or documents, or knowingly failing to comply with regulations protecting research participants. Fraud can be committed by individuals, institutions, or corporations; in the context of research, fraud often is motivated by considerations beyond financial gain. Institutional review boards (IRBs) are designed to ensure that researchers comply with human research subject protections, including conflict-of-interest controls, but IRBs may fail to do so if investigators avoid existing IRB processes or if IRB members do not take responsibility for addressing actual or potential conflicts of interest.

  • Copyright © 2007 The Cleveland Clinic Foundation. All Rights Reserved.
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Cleveland Clinic Journal of Medicine: 74 (3 suppl 2)
Cleveland Clinic Journal of Medicine
Vol. 74, Issue 3 suppl 2
1 Mar 2007
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Fraud, conflict of interest, and other enforcement issues in clinical research
Guy M. Chisolm, James G. Sheehan
Cleveland Clinic Journal of Medicine Mar 2007, 74 (3 suppl 2) S63-S67;

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Fraud, conflict of interest, and other enforcement issues in clinical research
Guy M. Chisolm, James G. Sheehan
Cleveland Clinic Journal of Medicine Mar 2007, 74 (3 suppl 2) S63-S67;
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  • Conflicts, compliance, and enforcement: Government priorities and initiatives
  • Protecting subjects without hampering research progress: Guidance from the Office for Human Research Protections
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