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Regulations last checked for updates: May 23, 2025
Title 21 - Food and Drugs last revised: May 19, 2025
All Titles
Title 21
Chapter I
Part 58 - PART 58—GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES
Subpart A [§ 58.1 - § 58.15] - Subpart A—General Provisions
Subpart B [§ 58.29 - § 58.35] - Subpart B—Organization and Personnel
Subpart C [§ 58.41 - § 58.51] - Subpart C—Facilities
Subpart D [§ 58.61 - § 58.63] - Subpart D—Equipment
Subpart E [§ 58.81 - § 58.90] - Subpart E—Testing Facilities Operation
Subpart F [§ 58.105 - § 58.113] - Subpart F—Test and Control Articles
Subpart G [§ 58.120 - § 58.130] - Subpart G—Protocol for and Conduct of a Nonclinical Laboratory Study
Subpart H - Subparts H-I [Reserved]
Subpart J [§ 58.185 - § 58.195] - Subpart J—Records and Reports
Subpart K [§ 58.200 - § 58.219] - Subpart K—Disqualification of Testing Facilities
authority:
21 U.S.C. 342
,
346
,
346
a,
348
,
351
,
352
,
353
,
355
,
360
,
360
b-360f,
360
h-360j,
371
,
379e
,
381
;
42 U.S.C. 216
,
262
,
263b
source:
43 FR 60013, Dec. 22, 1978, unless otherwise noted.
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