Current Good Manufacturing Practices (cGMPs) for Dietary Supplements

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The FDA regulates both finished dietary supplement products and dietary ingredients to ensure the safety and appropriate labeling of dietary supplements. These regulations focus on practices that ensure the identity, purity, quality, strength, and composition of dietary supplements. This lecture-based course provides training on 21 CFR 111, current Good Manufacturing Practices (cGMPs) in manufacturing, packaging, labeling or holding operations for dietary supplements.  Attention is given to the sixteen subparts, regulatory compliance, and maintaining a culture of quality.


  • Describe the regulation of dietary supplements
  • Recognize the role of cGMPs in the manufacture and testing processes
  • Identify departmental roles and required documentation
  • Understand the 16 subparts of 21 CFR Part 111
  • Participate in a simulated, controlled-product manufacturing process
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Course Features

  • Lectures 0
  • Hands-On Training 0
  • Duration 4.5 hours
  • Skill level All Levels
  • Wet Lab Yes
  • Max Students 24
  • Assessments Yes