21 CFR 111, 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?
Title 21 published on 2012-04-01
no entries appear in the Federal Register after this date.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].
It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.
