United States Food and Drug Administration (US FDA). Good Laboratory Practice (GLP) Final Rule[R]. North Miami:US FDA, 1978
United States Environmental Protection Agency (US EPA). 40CFR Part 160 Good Laboratory Practice Standards[EB/OL]. (1989-08-17)[2019-08-02]. https://www.govinfo.gov/content/pkg/CFR-2011-title40-vol24/xml/CF-R-20-11-title40-vol24-part160.xml
Germany Bundesinstitut für Risikobewertung (BFR). Conducting GLP Inspections in Germany Manual[EB/OL]. (2018-08-13)[2019-08-02]. https://www.bfr.bund.de/en/_glp_documents-70451.html
Ministry of Health, Labour and Welfare, Ministry of Economy Trade and Industry, Ministry of the Environment. Notice of the Good Laboratory Practice for Test Facilities Conducting Tests of New Chemical Substances:No.11-0331010.[EB/OL]. (2018-08-13)[2019-08-02]. https://www.nite.go.jp/data/000009018.pdf
日本环境省. GLP测试机构自查手册. GLP-IN-02.[EB/OL]. 第4版.[2019-08-02 ]. https://www.meti.go.jp/policy/chemical_management/kasinhou/files/about/laws/GLP-IN-02_04_2.pdf
United States Food and Drug Administration (US FDA). 21 CFR Part 58 Good Laboratory Practice for Nonclinical Laboratory Studies[EB/OL].(2019-09-19)[2019-12-01]. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?cfrpart=58
Seiler J P. Good Laboratory Practice-The Why and the How[M]. Springer, 2005:84-88
Piton A. Risk-based assessment applied to QA GLP audits. How to fulfill regulatory requirements while making the best use of our common sense, knowledge, talents, and resources[J]. Annali Dellistituto Superiore Di Sanità, 2008, 44(4):379