PAS-X MBR Design & Optimization for Pharmaceutical Manufacturing
Master Batch Records are the backbone of your manufacturing operations. They define how product gets made, how operators execute and how your facility stays compliant. But, too many MBRs are overcomplicated, inefficient or they are built by people who have never actually run a batch.
We design MBRs from the operator’s perspective: lean, logical and built for the people who use them every day. Whether you’re implementing PAS-X for the first time, migrating from a legacy system or fixing batch records that are slowing down production, we bring deep technical expertise and shop-floor experience to every project.
What We Deliver
↠ New MBR development for PAS-X implementations (versions 3.1.X through 3.3.X)
↠ MBR redesign and optimization to reduce batch execution time, eliminate unnecessary steps, and improve operator efficiency
↠ Modular, template-based design using able-to-validate building blocks that standardize common process steps across product families (faster to deploy, easier to update, more consistent)
↠ Legacy MES-to-PAS-X MBR migration including master data migration, process mapping, logic translation and functional gap analysis
↠ Versioning and lifecycle management to keep your batch records clean, controlled and audit-ready
↠ Integration support for material management, equipment registration, sampling workflows and ERP/LIMS connectivity
↠ Operator-focused design philosophy: we build systems for the people who actually use them
