L7 MES is the manufacturing execution system application within L7|ESP® for regulated pharmaceutical and advanced therapeutics production. It manages master batch records, electronic batch records, recipes, materials, samples, specifications, signatures, deviations, and quality review within connected manufacturing workflows. The datasheet introduces capabilities for dynamic process execution, conditional routing, review by exception, batch reporting, sample coordination with L7 LIMS, and integration with inventory and other L7|ESP applications across small-molecule, biologics, and cell and gene therapy manufacturing.
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