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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 F - Biologics |
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Part 606 - Current Good Manufacturing Practice for Blood and Blood Components |
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Subpart I - Records and Reports |
| § 606.160 - Records. |
| § 606.165 - Distribution and receipt; procedures and records. |
| § 606.170 - Adverse reaction file. |
| § 606.171 - Reporting of product deviations by licensed manufacturers, unlicensed registered blood establishments, and transfusion services. |