Title 21

PART 211 SUBPART E

Subpart E - Control of Components and Drug Product Containers and Closures

• 21 U.S.C. 321, 351, 352, 355, 360b, 371, 374; 42 U.S.C. 216, 262, 263a, 264.
• 43 FR 45077, Sept. 29, 1978, unless otherwise noted.

21:4.0.1.1.11.5.1.1	SECTION 211.80	211.80 General requirements.
21:4.0.1.1.11.5.1.2	SECTION 211.82	211.82 Receipt and storage of untested components, drug product containers, and closures.
21:4.0.1.1.11.5.1.3	SECTION 211.84	211.84 Testing and approval or rejection of components, drug product containers, and closures.
21:4.0.1.1.11.5.1.4	SECTION 211.86	211.86 Use of approved components, drug product containers, and closures.
21:4.0.1.1.11.5.1.5	SECTION 211.87	211.87 Retesting of approved components, drug product containers, and closures.
21:4.0.1.1.11.5.1.6	SECTION 211.89	211.89 Rejected components, drug product containers, and closures.
21:4.0.1.1.11.5.1.7	SECTION 211.94	211.94 Drug product containers and closures.

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