Paperless Manufacturing PAS-X MES

a woman in a lab environment working on PAS-X MES

Eliminate paper burdens for guided, error-free production. Switch to paper-on-glass production using PAS-X Electronic Batch Recording and Equipment Management.

Replace manual logbook maintenance with automated workflow-driven processes maintaining equipment and batch status tracking while operators efficiently work through the Electronic Batch Record.

In numbers

Speed to market

60%

Get life-saving therapies to patients faster by cutting your lead times by 60% and accelerating product releases through digitalized workflows.

Operational risk

80%

Protect your brand and patient safety by eliminating manual documentation errors and significantly reducing human-induced deviations by 80%.

Process quality

98%

Maximize your productivity with a 98% right-first-time factor, ensuring consistent product quality across every batch you produce.

Compliance

100%

Ensure your processes are 100% GMP-compliant, with fully protected audit trail records that permit no deletion or editing.

Transformation

60%

Accelerate your digital transformation and achieve 60% faster product launches with optimized, feasible work plans.

Benefits

Why choose PAS-X EBR and EQM

Intuitive graphical MBR design

Use a drag-and-drop tool with standardized, reusable building blocks to model any pharma or biotech activity without coding skills.

Automated equipment logbooks and tracking

Ensure only authorized, cleaned equipment is used on the shop floor with automated logbook population and real-time status monitoring.

Configurable approval workflows

Shorten your release cycles with configurable approval workflows and a dashboard that navigates you directly to deviations for faster review.

Reduced recipe maintenance

Use generic MBRs to define parameters instead of values, significantly reducing the total number of recipes you need to maintain.

Future-proof MES scaling

Start with paperless batch recording and scale later, with automated logbooks or resource management as your operational needs grow.

Global expert support

Access local support from our pharma software experts in over 100 locations worldwide, from Japan to Germany and the US.

Seamless ERP and automation integration

Ensure information exchange via ERP interfaces and bi-directional interfaces to the automation level for unified shop floor control.

PAS-X Electronic Batch Recording

Master your manufacturing processes with PAS-X EBR, designed to guide you through error-free production. You can easily build complex recipes using a graphical design tool with standardized, reusable blocks, no programming required.

Before you go live, use the simulation toolkit to test your workflows, ensuring they perform exactly as planned. During production, the system continuously monitors your data, blocking unauthorized entries to keep you compliant.

You can then shorten your release cycles through a dedicated dashboard that lets you focus only on exceptions, giving you total confidence in your batch documentation.

PAS-X Equipment Management

Take the guesswork out of asset readiness with PAS-X Equipment Management. You gain full control over the status of every production-related object through intuitive, web-based state diagrams that track cleaning, sterilization, and maintenance.

Integrated timers and counters automatically flag equipment as unusable once limits expire, preventing costly material waste and compliance risks. Your operators can verify asset status instantly via barcode scanning, ensuring they always use the right tool for the job.

With automated logbooks and powerful search filters, you can retrieve usage history in seconds during audits, replacing stacks of paper with digital certainty.

“We selected PAS-X MES because it is recognized as the world’s leading manufacturing execution system for pharma, biotech and cell & gene manufacturing.”
Krzysztof Stronski
Operations Director, SteriPack, Poland

Case study

SteriPack: Achieving auto-batch release in just 9 months

Leading contract manufacturer SteriPack implemented PAS-X MES to replace paper-based execution with digital processes across its packaging operations.

By utilizing PAS-X Electronic Batch Recording (EBR), SteriPack integrated its existing IT landscape, including asset and training management systems, to leverage industry-leading review-by-exception capabilities. This fast-track, out-of-the-box implementation was completed in only nine months, allowing the company to significantly lift productivity, improve time-to-market, and ensure total GxP compliance.

Read the case study

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.

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Downloads

Documentation

Brochure: PAS-X Electronic Batch Recording

Discover how to create and execute Master Batch Records to control, monitor, and document manufacturing processes in compliance with statutory provisions, with PAS-X EBR.

Brochure: PAS-X Equipment Management

Learn how to easily administer cleaning procedures and monitor equipment statuses for all production-related objects, with PAS-X Equipment Management.