Code of Federal Regulations · Subpart
Subpart F — Production And Process Control System: Requirements For Quality Control
21 C.F.R. pt. 111, subpt. F
- § 111.103 What Are The Requirements Under This Subpart F For Written Procedures?
- § 111.105 What Must Quality Control Personnel Do?
- § 111.110 What Quality Control Operations Are Required For Laboratory Operations Associated With The Production And Process Control System?
- § 111.113 What Quality Control Operations Are Required For A Material Review And Disposition Decision?
- § 111.117 What Quality Control Operations Are Required For Equipment, Instruments, And Controls?
- § 111.120 What Quality Control Operations Are Required For Components, Packaging, And Labels Before Use In The Manufacture Of A Dietary Supplement?
- § 111.123 What Quality Control Operations Are Required For The Master Manufacturing Record, The Batch Production Record, And Manufacturing Operations?
- § 111.127 What Quality Control Operations Are Required For Packaging And Labeling Operations?
- § 111.130 What Quality Control Operations Are Required For Returned Dietary Supplements?
- § 111.135 What Quality Control Operations Are Required For Product Complaints?
- § 111.140 Under This Subpart F, What Records Must You Make And Keep?