industrial HVAC/R solutions
Pharma Temperature Validation (2°C to 8°C)
Highly regulated pharmaceutical cold rooms require N+1 backup systems, calibrated digital data loggers, automatic alarm switchers, and DQ/IQ/OQ/PQ validation audits.
Dual refrigeration unit automatic switchover panels
FDA 21 CFR Part 11 compliant data logger setup
IQ/OQ/PQ technical documentation audits
Standby generator failover loops testing
Estimated Cost
Custom Validation Quote
*Standard pricing applies for diagnostic audits. Exact spare parts quoted on site.
Guaranteed WorkmanshipAll spare parts are genuine OEM components backed by warranty logs.
Our Service & Commissioning Process
We follow a strict mechanical diagnosis standard to ensure zero failures.
Phase 01
Conducting multi-point thermal mapping test holds
Phase 02
Testing automatic backup unit failover systems
Phase 03
Calibrating system alarm sirens and phone notifications
Phase 04
Compiling validation documentation