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Preserving Public Trust Accreditation and Human Research Participant Protection Programs (2001) / Chapter Skim
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Pages 124-130

The Chapter Skim interface presents what we've algorithmically identified as the most significant single chunk of text within every page in the chapter.
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From page 124...
... COMMENTARY on Standard 2.1: See Standard 1.2 2.2 The IRB(s) must identify to the appropriate institutional officials the resources it requires.
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From page 125...
... (e.g., behavioral research, clinical trials, epidemiological research, and research involving vulnerable populations or minority groups) will influence membership requirements.
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From page 126...
... Organizations should support appropriate training for IRB administration. This may include their attendance at andior participation in meetings or programs on the protection of individuals studied in research, acquisition of topic-oriented journals/books, and/or professional development such as certification through the ARENA Council for Certification of IRB Professionals (CCIP)
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From page 127...
... ; (4) Informed consent is sought from research participants or their authorized representatives unless waived by the IRB; (5)
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From page 128...
... (D) Requirements for the consent process, including the consent forms and their modifications (E)
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From page 129...
... (N) Reporting IRB findings to investigators, appropriate institutional officials, and appropriate federal or other regulatory agencies (O)
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From page 130...
... COMMENTARY on Standard 2.13: IRB minutes are fundamental parts of its record keeping activities. The minutes, together with other IRB documents, should enable a reader who was not present at the meeting to determine how and with what justifications the IRB arrived at its decisions.
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Key Terms

  • consent forms
  • irb minutes
  • informed consent
  • individuals studied
  • accreditation standards

  • research participants
  • authorized representative
  • expedited review
  • consent form
  • clinical trials

  • continuing review
  • irb policies
  • research involving
  • consent process
  • initial review

  • institutional official
  • obtaining informed
  • involving human
  • irb review
  • vulnerable populations

  • anticipated benefits
  • irb documents
  • consent requirements
  • applicable federal
  • research participant

  • appropriate institutional
  • written policies
  • perceived conflicts
  • institutional review
  • irb protocol


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