On-Demand Webinar: From Paper to Digital: Lean MES for Single-Use Bioprocessing
Paper-based SOPs and batch records are still the norm in many single-use facilities. But with increasing complexity — variable setups, evolving equipment, and strict regulatory requirements — paper often slows teams down. Manual recording introduces errors, complicates deviation management, and delays batch release, leaving operators and QA teams burdened by binders rather than empowered by data.
Explore how a lean MES approach offers a practical alternative. Rather than relying on monolithic systems, lean MES delivers lightweight, adaptable digital tools that fit the realities of single-use bioprocessing. These tools digitize SOPs and batch records, provide QA with real-time visibility, and improve traceability without the heavy overhead of traditional MES.
This session is especially valuable for manufacturing, QA, and digital transformation leaders in biopharma who are seeking ways to reduce paper dependency, accelerate release cycles, and improve efficiency in upstream operations.
What You Will Learn:
- Identify risks, inefficiencies, and delays caused by paper SOPs and batch records
- Explore how lean MES replaces paper with adaptable tools for single-use bioprocessing
- Learn practical steps to start small, digitize workflows, and build lasting efficiency