PAS-X Neo
The purpose-built, cloud-native MES that gives pharma and life sciences manufacturers a right-sized path to digital manufacturing.
Right from the start
Why PAS-X Neo
Right-sized
Start with what your site needs
Start with pre-defined proven pharma processes, and add more capability when you're ready.
Right first time
Records that stand up from the first batch
Built to support ALCOA+, FDA 21 CFR Part 11 and EU Annex 11, with audit trails, electronic signatures and enforced step order.
Right for your team
Easy to adopt, without the IT load
Fully managed in the cloud, with intuitive, guided workflows and pre-validated packages, so your team stays focused on production.
Right away
Fast time to value, with a target go-live of around two months
Pre-built process templates and pre-validated packages get your site from paper to its first digital batches quickly.
Benefits
Leave paper behind
Move batch records, and equipment and material status, from paper, logbooks and spreadsheets into one digital system, with fewer recording errors and less compliance risk.
Batch records ready for review
Data is captured as the work happens, so the batch record is ready for review when the batch ends, with exceptions flagged for review by exception.
Effort and costs that fit your site
Lean, standardized, cloud-native architecture lowers total cost of ownership, even with limited internal IT, validation or MES capacity.
Grow with confidence
Start small and scale, with access to the PAS-X portfolio and the wider Körber ecosystem.
PAS-X Neo features
Built to fit
Körber expertise
Guided from first step to full operation
Downloads
Documentation
Factsheet: PAS-X Neo
Explore whether PAS-X Neo fits your site: how to leave paper behind without doing everything at once, what your team gains, and how you can grow with PAS-X.
