
Overview
Specialized cleanroom HVAC with controlled temperature, humidity, filtration and pressurization. We design airflow patterns, HEPA layouts, differential pressures and recovery rates for pharma, labs and electronics. Compliances: ISO cleanroom classes, cGMP guidance (reference), NABL/USFDA expectations (as applicable). Benefits: Regulatory readiness, consistent product quality, lower contamination risk, validated environmental control. Why Choose Us: Expert detailing, DQ/IQ/OQ documentation support, particle/airflow testing, and training for operations.
Specifications
| Specification | Value |
|---|---|
| Classification | ISO class 5–9 / NABL/USFDA-aligned (as applicable) |
| Filtration | Pre/medium/HEPA stages |
| Pressures | Cascade pressurization logic |
| Air Changes | As per class/room function |
| Materials | Cleanroom-compatible finishes |
| Validation | Particle counts, recovery, smoke tests |