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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 |
| Part 600 - Biological Products: General |
| Part 601 - Licensing |
| Part 606 - Current Good Manufacturing Practice for Blood and Blood Components |
| Part 607 - Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices |
| Part 610 - General Biological Products Standards |
| Part 630 - Requirements for Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use |
| Part 640 - Additional Standards for Human Blood and Blood Products |
| Part 660 - Additional Standards for Diagnostic Substances for Laboratory Tests |
| Part 680 - Additional Standards for Miscellaneous Products |