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Code of Federal Regulations
Title 21
Chapter I
Subchapter C
Part 211
21 C.F.R. Part 211
Current Good Manufacturing Practice for Finished Pharmaceuticals
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A
General Provisions
B
Organization and Personnel
C
Buildings and Facilities
D
Equipment
E
Control of Components and Drug Product Containers and Closures
F
Production and Process Controls
G
Packaging and Labeling Control
H
Holding and Distribution
I
Laboratory Controls
J
Records and Reports
K
Returned and Salvaged Drug Products