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Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements
Law
CFR 21
Food and Drugs
Food and Drug Administration, Department of Health and Human Services
Food for Human Consumption
Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements
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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
I
Production and Process Control System: Requirements for the Batch Production Record
Subpart
J
Production and Process Control System: Requirements for Laboratory Operations
Subpart
K
Production and Process Control System: Requirements for Manufacturing Operations
Subpart
L
Production and Process Control System: Requirements for Packaging and Labeling Operations
Subpart
M
Holding and Distributing
Subpart
N
Returned Dietary Supplements
Subpart
O
Product Complaints
Subpart
P
Records and Recordkeeping