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?