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Preserving Public Trust Accreditation and Human Research Participant Protection Programs (2001) / Chapter Skim
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Pages 40-40

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From page 40...
... Thus, accreditation bodies need to develop standards or a subset of standards that embrace the independent IRB model. Independent IRBs can stop a trial, but they do not employ investigators or have authority over them in the same way that the faculty at an academic health center does.
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Key Terms

  • accreditation standards
  • independent irbs
  • accreditation bodies
  • clinical trials
  • initial review

  • ethical conduct
  • academic health
  • adverse events
  • subsequent report
  • fda regulations

  • growing fraction
  • independent irb
  • draft standards
  • research institution
  • develop standards

  • clinical trial
  • research review
  • clinical practice
  • adverse event
  • research oversight


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