21 CFR Subpart F
Production and Process Control System: Requirements for Quality Control
June 25, 2020
§
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?
Tried the LawStack mobile app?
Join thousands and try LawStack mobile for FREE today.
- Carry the law offline, wherever you go.
- Download CFR, USC, rules, and state law to your mobile device.
