CFR section
21 CFR 56.106(a): Registration
PART 56-INSTITUTIONAL REVIEW BOARDS · Subpart B-Organization and Personnel
Key facts
| Citation | 21 CFR 56.106(a) |
|---|---|
| Section | Registration |
| Part | PART 56-INSTITUTIONAL REVIEW BOARDS |
| Subpart | Subpart B-Organization and Personnel |
| Subchapter | 21 CFR A General |
| Product types cited | General |
| Regulation text (excerpt) | (a) Who must register? Each IRB in the United States that reviews clinical investigations regulated by FDA under sections 505(i) or 520(g) of the act and each IRB in the United States that reviews clinical investigations that are intended to support applications for research or marketing permits for FDA-regulated products must register at a site maintained by the Department of Health and Human Services (HHS). (A research permit under section 505(i) of the act is usually known as an… |
At a glance
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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.