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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter A - General |
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Part 50 - Protection of Human Subjects |
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Subpart B - Informed Consent of Human Subjects |
| § 50.20 - General requirements for informed consent. |
| § 50.21 - Effective date. |
| § 50.22 - Exception from informed consent requirements for minimal risk clinical investigations. |
| § 50.23 - Exception from general requirements. |
| § 50.24 - Exception from informed consent requirements for emergency research. |
| § 50.25 - Elements of informed consent. |
| § 50.27 - Documentation of informed consent. |