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Regulations last checked for updates: May 22, 2025
Title 21 - Food and Drugs last revised: May 19, 2025
All Titles
Title 21
Chapter I
Part 211 - PART 211—CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
Subpart A [§ 211.1 - § 211.3] - Subpart A—General Provisions
Subpart B [§ 211.22 - § 211.34] - Subpart B—Organization and Personnel
Subpart C [§ 211.42 - § 211.58] - Subpart C—Buildings and Facilities
Subpart D [§ 211.63 - § 211.72] - Subpart D—Equipment
Subpart E [§ 211.80 - § 211.94] - Subpart E—Control of Components and Drug Product Containers and Closures
Subpart F [§ 211.100 - § 211.115] - Subpart F—Production and Process Controls
Subpart G [§ 211.122 - § 211.137] - Subpart G—Packaging and Labeling Control
Subpart H [§ 211.142 - § 211.150] - Subpart H—Holding and Distribution
Subpart I [§ 211.160 - § 211.176] - Subpart I—Laboratory Controls
Subpart J [§ 211.180 - § 211.198] - Subpart J—Records and Reports
Subpart K [§ 211.204 - § 211.208] - Subpart K—Returned and Salvaged Drug Products
authority:
21 U.S.C. 321
,
351
,
352
,
355
,
360b
,
371
,
374
;
42 U.S.C. 216
,
262
,
263a
,
264
source:
43 FR 45077, Sept. 29, 1978, unless otherwise noted.
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