Code of Federal Regulations, Title 21, Three-Volume Clinical Trials Set — PDF
Update your library with the latest additions and revisions to:
- Volume 1: Parts 1-99 — Protection of Human Subjects
- Volume 5: Parts 300-499 —INDs — Responsibilities of Sponsors and Investigators
(FDA, Drugs for Human Use)
- Volume 8: Parts 800-1299 — Investigational Device Exemptions
(FDA, Medical Devices)
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