21 CFR Part 211
CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
June 25, 2020
Subpart
C
Buildings and Facilities
Subpart
F
Production and Process Controls
Subpart
I
Laboratory Controls
Subpart
A
General Provisions
Subpart
B
Organization and Personnel
Subpart
D
Equipment
Subpart
E
Control of Components and Drug Product Containers and Closures
Subpart
G
Packaging and Labeling Control
Subpart
H
Holding and Distribution
Subpart
J
Records and Reports
Subpart
K
Returned and Salvaged Drug Products
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