Pharma / Life Sciences
Overview
A life-sciences manufacturer in the I-85 corridor needed cleanroom HVAC and utilities brought under validated Siemens control, ready for computer system validation sign-off.
GMP production demanded audit-trailed logic, tight environmental control, and an HMI built to support CSV. The documentation burden was as critical as the code itself.
We developed audit-trailed S7-1500 logic for cleanroom HVAC, pressure cascades, and utilities, paired with a validated HMI. Every change was tracked, and the full design and test documentation package was prepared for the customer's CSV process.
Audit-trailed control delivered with full CSV documentation
Stable cleanroom pressure and environmental control
Validation package accepted without rework
The documentation was as good as the code. Our validation team had everything they needed.
Automation Manager · Life Sciences