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Current Good Manufacturing Practice for Blood and Blood Components
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Biologics
Current Good Manufacturing Practice for Blood and Blood Components
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Subpart
A
General Provisions
Subpart
B
Organization and Personnel
Subpart
C
Plant and Facilities
Subpart
D
Equipment
Subpart
E
Subpart E [Reserved]
Subpart
F
Production and Process Controls
Subpart
G
Additional Labeling Standards for Blood and Blood Components
Subpart
H
Laboratory Controls
Subpart
I
Records and Reports