21 CFR Part 56
PART 56—INSTITUTIONAL REVIEW BOARDS
- PART 56—INSTITUTIONAL REVIEW BOARDS
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter A—General
- Subpart A—General Provisions
- § 56.101 Scope.
- § 56.102 Definitions.
- § 56.103 Circumstances in which IRB review is required.
- § 56.104 Exemptions from IRB requirement.
- § 56.105 Waiver of IRB requirement.
- Subpart B—Organization and Personnel
- § 56.106 Registration.
- § 56.107 IRB membership.
- Subpart C—IRB Functions and Operations
- § 56.108 IRB functions and operations.
- § 56.109 IRB review of research.
- § 56.110 Expedited review procedures for certain kinds of research involving no more than minimal risk, and for minor changes in approved research.
- § 56.111 Criteria for IRB approval of research.
- § 56.112 Review by institution.
- § 56.113 Suspension or termination of IRB approval of research.
- § 56.114 Cooperative research.
- Subpart D—Records and Reports
- § 56.115 IRB records.
- Subpart E—Administrative Actions for Noncompliance
- § 56.120 Lesser administrative actions.
- § 56.121 Disqualification of an IRB or an institution.
- § 56.122 Public disclosure of information regarding revocation.
- § 56.123 Reinstatement of an IRB or an institution.
- § 56.124 Actions alternative or additional to disqualification.
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