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  • AHPA cGMP SOP Templates

AHPA cGMP SOP Templates

The dietary supplement current good manufacturing practice (cGMP) rule (21 CFR part 111) requires supplement manufacturers to establish and follow federally mandated current good manufacturing practice to ensure the quality of the dietary supplement. Customize these standard operating procedure (SOP) templates to help comply with cGMP requirements.

Browse cGMP SOP Templates by Category

General and Example SOP Templates and Supporting Documents

Document Control SOP Templates and Supporting Documents

Personnel (Part B) cGMP SOP Templates and Supporting Documents

Plant and Grounds (Part C) cGMP SOP Templates and Supporting Documents

Equipment and Utensils (Part D) cGMP SOP Templates and Supporting Documents

Quality Control Personnel (Part F) cGMP SOP Templates and Supporting Documents

Receipt of Components, Packaging and Labeling (Part G) cGMP SOP Templates and Supporting Documents

Manufacturing -- MMR and BPR (Parts H & I) SOP Templates and Supporting Documents

Laboratory Operations (Part J) SOP Templates and Supporting Documents

Manufacturing Operations (Part K) SOP Templates and Supporting Documents

Returned Dietary Supplements (Part N) SOP Templates and Supporting Documents

Product Complaints (Part O) SOP Templates and Supporting Documents


  • AHPA Guidance Documents
  • AHPA cGMP SOP Templates
  • Botanical Safety Handbook
  • Herbs of Commerce
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  • AHPA Hemp Lexicon
  • AHPA Guidance Policies
  • Code of Ethics, Business Practices & Trade Requirements
  • More...

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