What US 45 CFR 46.116 (Common Rule): General Requirements for Informed Consent requires
Section 46.116 of the Common Rule sets the general requirements for informed consent in federally conducted or supported human-subjects research…
This is a preview. The full record adds the complete summary, 10 workflow steps, 9 schema fields and 8 primary citations. Start a free trial or see pricing.
Pillar: Education & Research · Authority: US Department of Health and Human Services (HHS) - Office for Human Research Protections · Version: 1.0.0 · Last updated:
Primary source: https://www.ecfr.gov/current/title-45/part-46
SHA-256 integrity: 47e7139b3fdf37e34e263581dcf92937d188fc6af4d6740c26ab7287a9d819a8
Primary Citations — 8 traced to source
- US 45 CFR 46.116: General requirements for informed consent
- 46.116(a)(1): Before involving a human subject in research covered by this policy, an investigator shall obtain the legally effective informed consent of the subject or the subject's legally authorized representative
+ 6 more citations (full bibliography, deterministic workflow, actionable schema and crosswalks) included in the vault unlock — $0.01 via Skyfire / L402 / Direct Base USDC.
Access
- Discovery (free): /api/v1/nodes/us-45-cfr-46-116-common-rule-informed-consent.json — 6-field metadata
- Vault (full node): /api/v1/vault/nodes/us-45-cfr-46-116-common-rule-informed-consent.json — full 13-key payload, $0.01 USDC (L402/Skyfire/Direct Base)
- Canonical URL: https://bidda.com/intelligence/us-45-cfr-46-116-common-rule-informed-consent
- Back to registry: Browse all 10,102 compliance nodes