CFR section
21 CFR 56.115(a)(7): IRB records
PART 56-INSTITUTIONAL REVIEW BOARDS · Subpart D-Records and Reports
Key facts
| Citation | 21 CFR 56.115(a)(7) |
|---|---|
| Section | IRB records |
| Part | PART 56-INSTITUTIONAL REVIEW BOARDS |
| Subpart | Subpart D-Records and Reports |
| Subchapter | 21 CFR A General |
| Product types cited | General |
| Regulation text (excerpt) | (7) Statements of significant new findings provided to subjects, as required by § 50.25. |
At a glance
- 1–9 Inspections citing this section
- None 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.