PAS-X Savvy
Optimize your pharmaceutical processes with data analytics and end-to-end digital-twins based on real-time data. Our cloud-native platform integrates data management and AI to accelerate your time to market.
Turn fragmented bioprocess data into meaningful, actionable insights.
Why choose PAS-X Savvy
In numbers
Increase your yields
35%
Boost your biotech output. Digital twin implementation has proven to increase process yields by 35%, while reducing out-of-specification rates by 50%.
Faster release
40x
Accelerate your release cycles. Reduce batch record review times 40-fold, transforming a 4-week process into just 4 hours.
Improve compliance
50%
Maintain high quality standards. Decrease your out-of-specification rates by 50% through predictive analytics and smart process monitoring.
Benefits
Speed up your product launches
Shorten development cycles, mitigate launch risks and ensure robust data integrity through one integrated analytics platform.
Accelerate your lab analysis
Reduce redundant experiments with analysis ready data before every run, freeing up personnel capacity and lowering costs.
Trust your results every time
Ensure that all analyses are traceable and reproducible. Raw data is never modified, giving you reliable documentation.
Break down global data silos
Connect data across every operation, site, and department to create a shared understanding that drives better decisions.
PAS-X Savvy in action
PAS-X Savvy features
Your complete analytics toolkit
“Körber successfully helped Boehringer Ingelheim in their process characterization study using innovative end-to-end process models. This led to an efficient and scientifically sound establishment of a control strategy including specification driven in-process-control limits for CQAs and CPP.”
Boehringer Ingelheim Research Center, Vienna
Case studies
Connect your data
Körber expertise
Partnering for your success
Our team combines deep domain knowledge across IT, statistics, and bioprocess development to assist you with holistic data integration.
We leverage our deep expertise as the provider of the PAS-X MES Suite, recognized as the world's leading Manufacturing Execution System for pharma and biotech, to ensure your analytics layer connects seamlessly with your production environment. This foundation allows us to turn fragmented data into trusted, actionable insights that support faster development and compliant operations.
To ensure your success, we follow a proven, agile Ready-Fit-Build-Run implementation strategy tailored precisely to your needs. This customized approach ensures that your software adoption exceeds your data analytic expectations.
Master your bioprocess data
Learn how to achieve end-to-end visibility and successful process upscaling for faster, science-backed decisions in our PAS-X Savvy webinar.
Operational focus
Apply PAS-X Savvy to your workflows
Continued Process Verification (CPV)
Maintain your validated state effortlessly. Use statistical trending to monitor long-term performance and identify shifts before they impact your quality.
Automated Batch Record assembly
Eliminate manual data gathering. Automatically pull execution and quality data from your DCS and LIMS to accelerate your review and approval cycles.
Contextualized manufacturing data layer
Build a foundation for your AI applications. Harmonize raw data into an opinionated model that is ready for immediate reuse across your entire enterprise.
Design space management
Take control of your process parameters. Define, manage, and analyze your design spaces holistically across both development and manufacturing stages.
Downloads
Documentation
Brochure: PAS-X Savvy
Discover how to revolutionize the process of managing, analyzing, and reporting your pharma and biotech process data to create deeper insights.
Factsheet: PAS-X Savvy for bioprocess data management
Gain a holistic overview of your entire process chain to ensure robust understanding and faster tech transfer at any stage.
Factsheet: Integrated process modelling
Leverage PAS-X Savvy digital twins to achieve robust control strategies, reduce your Out-of-Specification rates, and optimize production yields
Factsheet: Successfully implementing PAS-X Savvy
See how PAS-X Savvy's implementation follows our proven Ready-Fit-Build-Run methodology for a successful and customized rollout at your site.
