21 CFR Subpart E - 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.