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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 607 - Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices |
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Subpart B - Procedures for Domestic Blood Product Establishments |
| § 607.20 - Who must register and submit a blood product list. |
| § 607.21 - Times for establishment registration and blood product listing. |
| § 607.22 - How to register establishments and list blood products. |
| § 607.25 - Information required for establishment registration and blood product listing. |
| § 607.26 - Amendments to establishment registration. |
| § 607.30 - Updating blood product listing information. |
| § 607.31 - Additional blood product listing information. |
| § 607.35 - Blood product establishment registration number. |
| § 607.37 - Public disclosure of establishment registration and blood product listing information. |
| § 607.39 - Misbranding by reference to establishment registration, validation of registration, or to registration number. |