Code of Federal Regulations · Part

Part 111 — Current Good Manufacturing Practice In Manufacturing, Packaging, Labeling, Or Holding Operations For Dietary Supplements

21 C.F.R. pt. 111

• 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