What US 21 CFR Part 50: Protection of Human Subjects requires
US 21 CFR Part 50 sets requirements for informed consent of human subjects in FDA-regulated clinical investigations of drugs, biologics, devices, and other products…
This is a preview. The full record adds the complete summary, 8 workflow steps, 16 schema fields and 5 primary citations. Start a free trial or see pricing.
Pillar: Pharmaceuticals & Life Sciences · Authority: US Food and Drug Administration (FDA) · Version: 1.0.0 · Last updated:
Primary source: https://www.ecfr.gov/current/title-21/chapter-I/subchapter-A/part-50
SHA-256 integrity: 26b4d4e3d00471962696eb253639832d58ccad0bf4f72178c87f28f7bfdaf0da
Primary Citations — 5 traced to source
- Title 21 Code of Federal Regulations Part 50 Protection of Human Subjects
- Title 21 Code of Federal Regulations Part 56 Institutional Review Boards
+ 3 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-21-cfr-part-50-protection-human-subjects.json — 6-field metadata
- Vault (full node): /api/v1/vault/nodes/us-21-cfr-part-50-protection-human-subjects.json — full 13-key payload, $0.01 USDC (L402/Skyfire/Direct Base)
- Canonical URL: https://bidda.com/intelligence/us-21-cfr-part-50-protection-human-subjects
- Back to registry: Browse all 10,102 compliance nodes