21 CFR Part 111
CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
June 25, 2020
Subpart
J
Production and Process Control System: Requirements for Laboratory Operations
Subpart
I
Production and Process Control System: Requirements for the Batch Production Record
Subpart
L
Production and Process Control System: Requirements for Packaging and Labeling Operations
Subpart
A
General Provisions
Subpart
B
Personnel
Subpart
C
Physical Plant and Grounds
Subpart
D
Equipment and Utensils
Subpart
E
Requirement to Establish a Production and Process Control System
Subpart
F
Production and Process Control System: Requirements for Quality Control
Subpart
G
Production and Process Control System: Requirements for Components, Packaging, and Labels and for Product That You Receive for Packaging or Labeling as a Dietary Supplement
Subpart
H
Production and Process Control System: Requirements for the Master Manufacturing Record
Subpart
K
Production and Process Control System: Requirements for Manufacturing Operations
Subpart
M
Holding and Distributing
Subpart
N
Returned Dietary Supplements
Subpart
O
Product Complaints
Subpart
P
Records and Recordkeeping
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