The US Food and Drug Administration promulgated the Good Laboratory Practice regulations for nonclinical laboratory studies in 1979, following the discovery that data in studies submitted in support ...

Good Laboratory Practice (GLP): is a set of principles intended to assure the quality and integrity of non-clinical laboratory studies that are intended to support research or marketing permits for ...

CARLSBAD, Calif., Jan. 24, 2023 (GLOBE NEWSWIRE) -- Qualigen Therapeutics, Inc. (“Qualigen” or “the Company,” Nasdaq: QLGN), a diversified life sciences company focused on developing ...

The Good Laboratory Practice Regulations (GLPs), developed in the late 1970s, were necessary because some of the research studies submitted to the US Food and Drug Administration (FDA) were poorly ...

Part 58 – Good Laboratory Practices for Non-Clinical Laboratory Studies Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals Part 820 – Quality System Regulation ...