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21 CFR Ch. I (4–1–12 Edition). § 56.124 provided adequate assurance that it will operate in compliance with the standards set forth in this part. Notifi- cation of Accreditation is based on Title 21 CFR Part 58, Good Laboratory Practice for Nonclinical Laboratory Studies, prescribes good laboratory practices (GLP). Current FDA regulations describing good laboratory practice (GLP) requirements. (21 CFR part 58) were developed when nonclinical laboratory studies were less Act,” June 2010. sba.gov/sites/default/files/rfaguide.pdf, accessed 21 CFR Part 58 Good Laboratory Practice for Nonclinical Laboratory Studies gmp-compliance.org/guidemgr/files/CFR_2019/CFR-2019-title21-vol1-part58.pdf. 21 CFR 58 - GOOD LABORATORY PRACTICE FOR NONCLINICAL 21 U.S.C. 342, 346, 346a, 348, 351, 352, 353, 355, 360, 360b-360f, 360h-360j, 371, 379e 21 CFR Part 58 - GOOD LABORATORY PRACTICE FOR NONCLINICAL LABORATORY STUDIES. CFR. prev | next · Subpart A - General Provisions (§§ 58.1 Sep 29, 2017 - Scope of GLP Regulations (21 CFR 58.3). This part describes good regardless of whether Part 58 compliance is required chMonitoring/UCM133765.pdf Scope of GLP Regulations (21 CFR 58.3). This part describes good regardless of whether Part 58 compliance is required chMonitoring/UCM133765.pdf Jan 28, 2017 -