SCADA
Supervision and control of your plant, line, or machine
Software that adapts to every project
One single platform, configurable by module depending on the plant.
Proven security and reliability
A single platform that adapts to the needs of each project. After-sales support provided directly by the expert developers of the system itself, at a response speed that's hard to match.
100% web
Accessible from any device, using the most mature technology for unmatched stability.
Proven experience
Large-scale pharmaceutical projects delivered with our partner RSD Engineering.
Upfront study and planning
A close, personal level of service thanks to our own project planning system.
Software architecture
Applications built for a long service life through a modular, robust approach.
Built for GMP environments
If you manufacture pharmaceutical or healthcare product, your software needs to pass an audit. Ours was built ready for it.
Stable by design
A robust system, built to run for years without surprises.
Reliable communications
Drivers tested on real-world projects.
Audit trail and traceability
Every action is logged: who, what, and when (ALCOA+ integrity).
Electronic records
Users, roles, and signatures aligned with EU GMP Annex 11 / 21 CFR Part 11.
Full GxP documentation
URS, specifications, and IQ/OQ support, already written.
Batch and cycle reports
Ready for quality to review and archive.
How is a SCADA contracted?
We start with a plant visit and a joint URS: what the system needs to do, in black and white. Once the URS is closed, scope and budget are closed too.
What isn't recorded never happened. What isn't controlled eventually fails.