CFR section
21 CFR 56.107(e): IRB membership
PART 56-INSTITUTIONAL REVIEW BOARDS · Subpart B-Organization and Personnel
Key facts
| Citation | 21 CFR 56.107(e) |
|---|---|
| Section | IRB membership |
| Part | PART 56-INSTITUTIONAL REVIEW BOARDS |
| Subpart | Subpart B-Organization and Personnel |
| Subchapter | 21 CFR A General |
| Product types cited | Devices, Drugs, General |
| Regulation text (excerpt) | (e) No IRB may have a member participate in the IRB's initial or continuing review of any project in which the member has a conflicting interest, except to provide information requested by the IRB. |
At a glance
- 10–99 Inspections citing this section
- 1–9 Warning letters citing this section
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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.