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
Holding time: the study sets the limit; the routine is where it fails
RDC 658/2022 (art. 274) requires stability of intermediates and bulk. The real cost shows up when the limit exists in the report and disappears on the shop floor.
The electronic batch record: enforcement, not just the removal of paper
An EBR that only replaces paper buys very little. The value is a process enforced while it runs — and that has design costs worth understanding before you specify one.
Computerised system validation without the paperwork spiral
GAMP 5 asks for effort proportional to risk, yet most validation packages scale with page count instead. What a risk-based approach changes in practice, and what it does not excuse.
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