Part 211 — Current Good Manufacturing Practice for Finished Pharmaceuticals
Subpart A — General Provisions
Subpart B — Organization and Personnel
Subpart C — Buildings and Facilities
Subpart E — Control of Components and Drug Product Containers and Closures
- § 211.80— General requirements.
- § 211.82— Receipt and storage of untested components, drug product containers, and closures.
- § 211.84— Testing and approval or rejection of components, drug product containers, and closures.
- § 211.86— Use of approved components, drug product containers, and closures.
- § 211.87— Retesting of approved components, drug product containers, and closures.
- § 211.89— Rejected components, drug product containers, and closures.
- § 211.94— Drug product containers and closures.
Subpart F — Production and Process Controls
Subpart G — Packaging and Labeling Control
Subpart H — Holding and Distribution
Subpart I — Laboratory Controls
Subpart J — Records and Reports
Subpart K — Returned and Salvaged Drug Products