CFR section
21 CFR 56.115(a)(1): IRB records
PART 56-INSTITUTIONAL REVIEW BOARDS · Subpart D-Records and Reports
Key facts
| Citation | 21 CFR 56.115(a)(1) |
|---|---|
| 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) | (1) Copies of all research proposals reviewed, scientific evaluations, if any, that accompany the proposals, approved sample consent documents, progress reports submitted by investigators, and reports of injuries to subjects. |
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.