Part 225—Protection of Human Subjects

Sections

• § 225.101
  § 225.101 To what does this policy apply?
• § 225.102
  § 225.102 Definitions for purposes of this policy.
• § 225.103
  § 225.103 Assuring compliance with this policy—research conducted or supported by any Federal department or agency.
• § 225.104
  § 225.104 Exempt research.
• § 225.107
  § 225.107 IRB membership.
• § 225.108
  § 225.108 IRB functions and operations.
• § 225.109
  § 225.109 IRB review of research.
• § 225.110
  § 225.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
• § 225.111
  § 225.111 Criteria for IRB approval of research.
• § 225.112
  § 225.112 Review by Institution
• § 225.113
  § 225.113 Suspension or Termination of IRB Approval of Research.
• § 225.114
  § 225.114 Cooperative Research.
• § 225.115
  § 225.115 IRB Records.
• § 225.116
  § 225.116 General Requirements for Informed Consent.
• § 225.117
  § 225.117 Documentation of informed consent.
• § 225.118
  § 225.118 Applications and proposals lacking definite plans for involvement of human subjects.
• § 225.119
  § 225.119 Research undertaken without the intention of involving human subjects.
• § 225.120
  § 225.120 Evaluation and disposition of applications and proposals for research to be conducted or supported by a Federal department or agency.
• § 225.121
  § 225.121 [Reserved]
• § 225.122
  § 225.122 Use of Federal funds.
• § 225.123
  § 225.123 Early termination of research support: Evaluation of applications and proposals.
• § 225.124
  § 225.124 Conditions.
• §§ 225.105-225.106
  §§ 225.105-225.106 [Reserved]