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Title 21

Displaying title 21, up to date as of 9/22/2021. Title 21 was last amended 9/21/2021.
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Title 21 Food and Drugs Part / Section
Chapter I Food and Drug Administration, Department of Health and Human Services 1 – 1299
Subchapter F Biologics 600 – 680
Part 600 Biological Products: General 600.2 – 600.90
Subpart A General Provisions 600.2 – 600.3
Subpart B Establishment Standards 600.10 – 600.15
Subpart C Establishment Inspection 600.20 – 600.22
Subpart D Reporting of Adverse Experiences 600.80 – 600.90
Part 601 Licensing 601.2 – 601.95
Part 606 Current Good Manufacturing Practice for Blood and Blood Components 606.3 – 606.171
Part 607 Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices 607.1 – 607.80
Subpart A General Provisions 607.1 – 607.7
Subpart B Procedures for Domestic Blood Product Establishments 607.20 – 607.39
Subpart C Procedures for Foreign Blood Product Establishments 607.40
Subpart D Exemptions 607.65
Subpart E Establishment Registration and Product Listing Of Licensed Devices 607.80
Part 610 General Biological Products Standards 610.1 – 610.68
Part 630 Requirements for Blood and Blood Components Intended for Transfusion or for Further Manufacturing Use 630.1 – 630.40
Subpart A General Provisions 630.1 – 630.3
Subpart B Donor Eligibility Requirements 630.5 – 630.35
Subpart C Donor Notification 630.40
Part 640 Additional Standards for Human Blood and Blood Products 640.1 – 640.130
Part 660 Additional Standards for Diagnostic Substances for Laboratory Tests 660.1 – 660.55
Part 680 Additional Standards for Miscellaneous Products 680.1 – 680.3
§ 680.1 Allergenic Products.
§ 680.2 Manufacture of Allergenic Products.
§ 680.3 Tests.