《FDA 21CFR PART 111 & PART 117》膳食补充剂的生产、包装、标签或贮存操作的良好操作规范 和 食品现行良好操作规范和危害分析及基于风险的预防性控制措施 FDA 21CFR PART 111 & PART 117
《FDA 21 CFR Part 117 Subpart B》FDA 21 CFR Part 117 Subpart B, Current Good Manufacturing Practice FDA 21 CFR Part 117 Subpart B
《FDA 21CFR820》Quality System (QS) Regulation/Medical Device Good Manufacturing Practices FDA 21CFR820
《FDA GMPC》Good Manufacturing Practice Cosmetic FDA GMPC
《FDA QSR 820》FDA 21 CFR Part 820, Quality System (QS) Regulation/Medical Device Good Manufacturing Practices FDA QSR 820
《FDA 21 CFR Part 211》Current Good Manufacturing Practice for Finished Pharmaceuticals FDA 21 CFR Part 211
《FDA 21 CFR Part 111》cGMP Regulations and Controls are Used for Manufacturing, Processing, Packing, or Holding Dietary Supplements FDA 21 CFR Part 111
《FDA 21CFR110》Current Good Manufacturing Practice in Manufacturing, Packing, or Holding Human Food FDA 21CFR110
《FDA 21CFR117》Current Good Manufacturing Practice (GMP), Hazard Analysis, and Risk-Based Preventive Controls for Human Food FDA 21CFR117
《FDA 21 CFR Part 117》Current Good Manufacturing Practice, Hazard Analysis, and Risk-Based Preventive Controls for Human Food FDA 21 CFR Part 117