CFR section
21 CFR 56.115(a)(5): IRB records
PART 56-INSTITUTIONAL REVIEW BOARDS · Subpart D-Records and Reports
Key facts
| Citation | 21 CFR 56.115(a)(5) |
|---|---|
| Section | IRB records |
| Part | PART 56-INSTITUTIONAL REVIEW BOARDS |
| Subpart | Subpart D-Records and Reports |
| Subchapter | 21 CFR A General |
| Product types cited | Devices, Drugs, General |
| Regulation text (excerpt) | (5) A list of IRB members identified by name; earned degrees; representative capacity; indications of experience such as board certifications, licenses, etc., sufficient to describe each member's chief anticipated contributions to IRB deliberations; and any employment or other relationship between each member and the institution; for example: full-time employee, part-time employee, a member of governing panel or board, stockholder, paid or unpaid consultant. |
At a glance
- 100–999 Inspections citing this section
- 10–99 Warning letters citing this section
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About CFR sections cited by the FDA
Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.