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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 630 - Requirements for Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use |
Part 630 - Requirements for Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use
| Subpart A - General Provisions |
| § 630.1 - Purpose and scope. |
| § 630.3 - Definitions. |
| Subpart B - Donor Eligibility Requirements |
| § 630.5 - Medical supervision. |
| § 630.10 - General donor eligibility requirements. |
| § 630.15 - Donor eligibility requirements specific to Whole Blood, Red Blood Cells and Plasma collected by apheresis. |
| § 630.20 - Exceptions for certain ineligible donors. |
| § 630.25 - Exceptions from certain donor eligibility requirements for infrequent plasma donors. |
| § 630.30 - Donation suitability requirements. |
| § 630.35 - Requalification of previously deferred donors. |
| Subpart C - Donor Notification |
| § 630.6 - Donor notification. |
| § 630.40 - Requirements for notifying deferred donors. |