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Biologics
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Biologics
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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