CFR section
21 CFR 56.106(c): Registration
PART 56-INSTITUTIONAL REVIEW BOARDS · Subpart B-Organization and Personnel
Key facts
| Citation | 21 CFR 56.106(c) |
|---|---|
| Section | Registration |
| Part | PART 56-INSTITUTIONAL REVIEW BOARDS |
| Subpart | Subpart B-Organization and Personnel |
| Subchapter | 21 CFR A General |
| Product types cited | Devices, General |
| Regulation text (excerpt) | (c) When must an IRB register? Each IRB must submit an initial registration. The initial registration must occur before the IRB begins to review a clinical investigation described in paragraph (a) of this section. Each IRB must renew its registration every 3 years. IRB registration becomes effective after review and acceptance by HHS. |
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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.