Regulations.gov document
Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors
Other · FDA-2006-D-0031 · posted Aug 16, 2023
Key facts
| Document ID | FDA-2006-D-0031-0139 |
|---|---|
| Title | Informed Consent Guidance for IRBs, Clinical Investigators, and Sponsors |
| Document type | Other |
| Subtype | Guidance |
| Agency | FDA |
| Docket | FDA-2006-D-0031 |
| Posted | Aug 16, 2023 |
| Comment period opens | Aug 16, 2023 |
At a glance
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