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Current Good Manufacturing Practice in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Food for Human Consumption
  6. 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

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