L7 MES
a comprehensive manufacturing execution system for the precision therapeutics workflow
challenging the MES status quo
The manufacturing of pharmaceutical products is fraught with complexity and time constraints, frequently leading to delays, deviations, and escalating costs. Traditional methods rely on cumbersome, paper-based ecosystems and inflexible electronic systems, further compounded by non-compliant spreadsheets that create bottlenecks and delay product releases.
introducing L7 MES
Efficient Recipe Management
Rapid configuration of Master Batch Records, Intermediates, and Drug Product recipes.
Enhanced Operational Control
Supports configurable electronic signatures, sample plan management, and label reconciliation.
Comprehensive Documentation Integration
Enables Electronic Batch Records (EBR), Bill of Materials (BOM), Sample Plan Management, Specifications, Quality Review, Signature Sign-Off, and automatic Batch Reports.
L7 MES outperforms traditional manufacturing execution systems
L7 MES is part of the L7|ESP unified platform
L7 MES is integrated into the L7|ESP unified platform, sharing a common database with LIMS and inventory systems. It leverages the existing L7|ESP workflow configurations to accurately represent and manage the manufacturing process. Throughout production, it collects samples to be analyzed by LIMS. Additionally, L7|ESP supports enhancements with data trending and charting tools, enabling both single-batch and cross-batch analysis and reporting.
L7 MES app
datasheet
L7|ESP
brochure
