Dietary Supplement Master Handbook

Over 300 pages of guidance and regulations to ensure your compliance is up to date!

US FDA Title 21 CFR Parts:

• Part 11 - Electronic Records; Electronic Signatures with Scope and Application
• Part 110 - CGMP in Manufacturing, Packing, or Holding Human Food
• Part 111 - CGMP in Manufacturing, Packaging, Labeling, or Holding Operations for Dietary Supplements
• Part 117 - CGMP, Hazard Analysis, and Risk-Based Preventive Controls for Human Food
• Dietary Supplements Overview Guidance
• Dietary Supplements Guidance Handbook
• Dietary Supplements FAQ Reporting and Recordkeeping
• Dietary Supplements Labeling Requirements

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DietaryMaster-C-251217