Improve your production performance and compliance
The challenges for pharmaceutical and biopharmaceutical manufacturers increase with fewer blockbuster drugs, emerging markets, shorter time-to-market and increased regulatory complexity. Global players are looking to harmonize and optimize their IT systems, while mid-sized companies are focusing on standardized MES products.
Werum’s manufacturing IT solutions cover all these needs. The core of our offering is the PAS-X manufacturing execution system (MES) that combines software, content and services out of the box tailored for commercial manufacturing processes in pharma and biotech. Specific IT solutions are available for manufacturing operations such as process development, packaging and KPI/OEE. You can gradually extend these solutions until you benefit from a full-scope PAS-X MES.
We stand by our customers' site and, step by step, guide them through their MES project. From the very beginning we ask just the right questions to provide the right solution – based on our standard software product and our service and content packages, in a fast and targeted manner. We can rely on our unique implementation method, a guarantee for the success of your project!
Full coverage of pharma & biotech production
PAS-X supports all major pharmaceutical industry segments, e.g. for vaccines, biopharmaceuticals, solids, liquids and other manufacturing operations.
PAS-X covers the product lifecycle in pharmaceutical and biopharmaceutical manufacturing from process development to commercial production and packaging.
High performance, quality and compliance
Functionally complete MES solution for pharma- and biomanufacturing
To enable you to assert yourself on the highly competitive pharmaceutical market and to focus on your core business, we provide a complete MES solution ready for deployment.
Empowering Pharma 4.0
Systems, equipment, and personnel have become increasingly interconnected in the digital economy, offering new opportunities for the pharma and biotech industries. Together with our fellow Medipak Systems companies and other partners, Werum IT Solutions is working on innovative solutions to make Industrie 4.0 a reality in pharma.
Plug & Produce with PAS-X
Our Plug & Produce solution allows a fast and easy integration of machines and automation systems into a pharmaceutical production environment – a prerequisite for the implementation of many Industrie 4.0 solutions.
With K.ME-IN, Werum offers a smart biometric authentication solution for its market-leading PAS-X Manufacturing Execution System. Users can thus securely and seamlessly authenticate to systems, devices and machines via biometric means such as fingerprint, iris scan, face recognition or a combination of those.
Cell & Gene therapy with PAS-X MES
Werum’s PAS-X MES targets the key challenges for cell therapy manufacturers, managing complex processes and controlling the chain of identity.
Shop floor performance booster
PAS-X KPI is a lean, standalone software product that provides live monitoring of manufacturing and packaging lines, improving shop floor performance at pharmaceutical and biotech facilities.
Reliable and easy-to-operate weighing processes
Simplified creation and management of MBRs
Your manufacturing processes are described with complex or a huge number of master batch records? PAS-X Master Batch Records drastically simplifies your MBR creation.
Integrated IT solution for packaging
Compliance with anti-counterfeiting requirements
PAS-X Track & Trace Serialization Aggregation provides serialization and aggregation functionality for your packaging processes to cover anti-counterfeiting requirements.
Unlock the potential of your shop floor data
PAS-X Evaluations helps you to unlock the full potential of your shop floor data. Use your data to continuously improve manufacturing processes and to meet regulatory compliance requirements.
Efficient management of regulatory information with RImanager
Centralized Regulatory Information Management (RIM) solution enabling you to efficiently manage your master data and to plan and track related regulatory data, activities, processes, submissions and commitments.