{
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  "title": "US 21 CFR Part 50: Protection of Human Subjects",
  "domain": "Pharmaceuticals & Life Sciences",
  "version": "1.0.0",
  "last_updated": "2026-05-31",
  "bluf": "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…",
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