cfr_sections: 21:21:1.0.1.1.22.3.98.1

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section_id	title_number	title_name	chapter	subchapter	part_number	part_name	subpart	subpart_name	section_number	section_heading	agency	authority	source_citation	amendment_citations	full_text
21:21:1.0.1.1.22.3.98.1	21	Food and Drugs	I	A	58	PART 58—GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES	C	Subpart C—Facilities	58.41	§ 58.41 General.	FDA	21 U.S.C. 342, 346, 346a, 348, 351, 352, 353, 355, 360, 360b-360f, 360h-360j, 371, 379e, 381; 42 U.S.C. 216, 262, 263b-263n.	43 FR 60013, Dec. 22, 1978, unless otherwise noted.	[52 FR 33780, Sept. 4, 1987]	Each testing facility shall be of suitable size and construction to facilitate the proper conduct of nonclinical laboratory studies. It shall be designed so that there is a degree of separation that will prevent any function or activity from having an adverse effect on the study.