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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 |
Part 607 - Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices
| Subpart A - General Provisions |
| § 607.1 - Scope. |
| § 607.3 - Definitions. |
| § 607.7 - Establishment registration and product listing of blood banks and other firms manufacturing human blood and blood products. |
| 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. |
| Subpart C - Procedures for Foreign Blood Product Establishments |
| § 607.40 - Establishment registration and blood product listing requirements for foreign blood product establishments. |
| Subpart D - Exemptions |
| § 607.65 - Exemptions for blood product establishments. |
| Subpart E - Establishment Registration and Product Listing Of Licensed Devices |
| § 607.80 - Applicability of part 607 to licensed devices. |