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# Info Collection on Good Lab Practices
- URL: https://www.fdaweb.com/info-collection-on-good-lab-practices/
- Published: 2023-08-08T12:00:00.000Z
- Updated: 2026-09-14T18:49:00.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5155053

*Federal Register* notice: FDA is seeking comments on an information collection extension entitled “Good Laboratory Practice Requirements for Nonclinical Laboratory Studies — 21 CFR Part 58.” The collection supports agency regulations that require medical product manufacturers to adhere to good laboratory practices (GLPs) for nonclinical laboratory studies. The GLPs specify minimum standards for the proper conduct of safety testing and contain sections on facilities, personnel, equipment, standard operating procedures, test and control articles, quality assurance, protocol and study conduct, records and reports, and laboratory disqualification. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2023-08-08/pdf/2023-16925.pdf?ref=fdaweb.com).