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- Digital Manufacturing
- Define & schedule manufacturing
Define and schedule manufacturing
PAS-X MES enables you to digitalize recipes and optimize production schedules by automated planning to achieve faster batch release, higher quality, and full regulatory compliance across your operations.

Eliminate operational bottlenecks caused by paper-based workflows to boost your throughput and efficiency
In numbers
Speed to market
60%
Get essential treatments to patients faster by cutting your lead times by 60% and accelerating product releases through digitalized workflows.
Operational rysk
80%
Protect your brand and patient safety by eliminating manual documentation errors and significantly reducing human-induced deviations by 80%.
Asset uptime
98%
You reach up to 98% of machine and equipment utilization by synchronizing production orders with the real availability of your business assets.
Order backlogs
60%
Clear production bottlenecks and reduce order backlogs by 60% by generating feasible, optimized work plans.
Transformation
15%
Achieve a 15% internal lead time reduction for product transformation through precision scheduling of production activities.
Planning time
50%
Reduce the time spent on production planning by half through automated scheduling tools and customizable heuristic rules.
Benefits
Why choose PAS-X MBR and Scheduler
Spend less time on recipe maintenance
Use generic MBRs to significantly reduce the number of recipes you need to design and maintain for your production lines.
Eliminate human errors in your production
Protect your process quality with automated data checks that catch manual entry errors before they lead to costly batch deviations.
Always be ready for inspections
Gain peace of mind with fully automated documentation that records every production and review step for total regulatory traceability.
Keep your production moving during disruptions
Respond instantly to unforeseen events with real-time shop floor re-planning that keeps your throughput steady and equipment active.
Secure your regulatory compliance
Reduce your compliance risk by using a system designed to meet strict pharmaceutical industry requirements for GxP and data integrity.
Design your recipes with ease
Accelerate your digital transformation by building complex electronic workflows using an intuitive drag and drop MBR design tool.

PAS-X MBR
PAS-X MBR transforms your manual recipe management into a dynamic digital environment using a graphical workflow and material flow engine. Purpose-built for pharma, biotech and cell & gene manufacturing operations, our intuitive drag and drop interface, supported by pre-defined content libraries, makes it easy for your team to build compliant electronic workflows.
With generic MBRs, you can run multiple orders from a single design, while electronic approval workflows ensure seamless, GxP-compliant execution. PAS-X MBR eliminates paper-based inefficiencies and ensures full regulatory traceability for every batch.

PAS-X MBR Services
Unlock efficiency and accelerate your MES project success with our flexible expert support services. We offer three tailored service models to meet your unique needs:
- Managed Services: Delegate the entire MBR design process to our experts, from concept to delivery and go-live support.
- Help Desk: Gain continuous assistance through best practice workshops, regular meetings, and a centralized ticketing system with 48-hour response times.
- Health Check: Receive a comprehensive expert analysis of your MBR design against 35 critical criteria before production begins to minimize risk and identify optimizations.

PAS-X Scheduler
PAS-X Scheduler brings intelligence to your production planning by synchronizing operations with the real as-is status of the shop floor. Instead of static plans, you can generate optimized schedules using customizable heuristic rules that prioritize cost reduction or lead time minimization.
The system provides total visibility, identifying delivery risks through configurable alarms and dynamic pegging. By accounting for the real availability of machines and manpower, it helps you reach near-total equipment utilization. When disruptions occur, our software allows for immediate recalculation to keep your plant agile.
Why PAS-X MES?
Learn how our state-of-the-art Manufacturing Execution System saves time, saves effort, and avoids risk in your pharma factory while ensuring full compliance.
Master the 5 principles of MBR design
Read our white paper to discover how digital recipe design secures long-term MES success to ensure lean, efficient, and compliant production processes.
Downloads
Documentation
Brochure: PAS-X MBR Services
Discover how our MBR services can accelerate your MES project and cut costs.
Brochure: PAS-X Scheduler
See how to generate optimized production plans that reduce lead times and maximize asset utilization.



