Federal (United States) · Regulations
Subpart F — Production and Process Control System: Requirements for Quality Control
11 sections
11 sections
- 21 C.F.R. § 111.103What are the requirements under this subpart F for written procedures?
- 21 C.F.R. § 111.105What must quality control personnel do?
- 21 C.F.R. § 111.110What quality control operations are required for laboratory operations associated with the production and process control system?
- 21 C.F.R. § 111.113What quality control operations are required for a material review and disposition decision?
- 21 C.F.R. § 111.117What quality control operations are required for equipment, instruments, and controls?
- 21 C.F.R. § 111.120What quality control operations are required for components, packaging, and labels before use in the manufacture of a dietary supplement?
- 21 C.F.R. § 111.123What quality control operations are required for the master manufacturing record, the batch production record, and manufacturing operations?
- 21 C.F.R. § 111.127What quality control operations are required for packaging and labeling operations?
- 21 C.F.R. § 111.130What quality control operations are required for returned dietary supplements?
- 21 C.F.R. § 111.135What quality control operations are required for product complaints?
- 21 C.F.R. § 111.140Under this subpart F, what records must you make and keep?