The digital backbone of regulated manufacturing.
T2 Software helps Life Sciences manufacturers digitize operations — from batch record to release — with NEO, an enterprise platform built for GxP environments.
Complete digital transformation. Not just software.
We design, implement, validate and operate the systems that run regulated production — so quality, engineering and operations work from a single digital thread.
One platform, from shop floor to release.
NEO connects execution, quality and equipment in a single system of record for manufacturing.
We deliver projects, not licenses.
Every deployment includes the engineering, validation and infrastructure needed to run in production — end to end.
- 01ImplementationFrom process mapping to deployment, led by engineers who know GxP manufacturing.
- 02ValidationCSV documentation and execution aligned with GAMP 5.
- 03TrainingOperators, reviewers and administrators ready from day one.
- 04Go LiveCutover to production with our engineers beside your team at every step.
- 05HypercareIntensive post-go-live support until the operation runs stable on its own.
Latest insights
Complete batch record before review, not during it
The record does not always reach review blank. Often it arrives almost complete: the equipment used in one step is not identified, a weighing was entered at the end of the shift, a verification signature was left for later, an in-process result was copied by hand from a printout. Each gap looks small. Together they leave quality review reconstructing what happened instead of checking what was…
ALCOA+ on the floor: the reviewed record has to be what the plant generated
On the floor, a data integrity failure does not always start with a missing lab checklist. The shift generates injections, instrument printouts, equipment logbook entries and sampling records. The dossier that goes forward for release can show something else: injections that are missing, a copy instead of the original, raw data that does not match the batch record or the certificate of…
AI by risk tier: assist is not a GMP decision
On the floor, the failure mode is rarely "someone used AI". It is quieter: a generative suggestion for a deviation narrative, a cleaning hold, or a critical process parameter is treated as if it were already a GMP decision. The shift closes. The batch record moves. A responsible, trained person sees a polished text, not the gap between assist and decide.
Let’s digitize your operation.
Talk to our engineers about your digital manufacturing roadmap — from a single line to a global rollout.
Talk to an expert