Toward a more comprehensive approach to protecting human subjects: the interface of data safety monitoring boards and institutional review boards in randomized clinical trials.

Authors

Gordon, Valery; Sugarman, Jeremy; Kass, Nancy;

Keywords

  • Advisory Committees
  • Clinical Trials Data Monitoring Committees
  • Committee Membership
  • Drug Industry
  • Ethical Review
  • Ethics
  • Ethics Committees
  • Ethics Committees, Research
  • Federal Government
  • Government
  • Government Regulation
  • Guidelines as Topic
  • Human Experimentation
  • Multicenter Studies as Topic
  • National Institutes of Health (U.S.)
  • Organization and Administration
  • Random Allocation
  • Reference Standards
  • Research Design
  • Risk
  • Risk Assessment
  • Social Control, Formal
  • United States

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