21 CFR Subpart F - Subpart F—Production and Process Control System: Requirements for Quality Control
- § 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?