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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 D - Drugs for Human Use |
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Part 320 - Bioavailability and Bioequivalence Requirements |
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Subpart A - General Provisions |
| § 320.1 - Definitions. |