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Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Biologics
Establishment Registration and Product Listing for Manufacturers of Human Blood and Blood Products and Licensed Devices
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Subpart
A
General Provisions
Subpart
B
Procedures for Domestic Blood Product Establishments
Subpart
C
Procedures for Foreign Blood Product Establishments
Subpart
D
Exemptions
Subpart
E
Establishment Registration and Product Listing Of Licensed Devices