Cleanroom environments at PES Pharma are engineered as integrated systems where air quality, pressure relationships, and environmental stability support production requirements.
Our cleanroom engineering addresses:
PES Pharma
Cleanrooms exceed ISO 5, 7, 8, and CNC—not merely comply. Seismiccertified, Modular Pharma, and Human-Centered designs define our approach.
OEB 1–5
From low toxicity to highly potent APIs contained weighing stations, isolators, split valves, and negative pressure zones ensure operator protection at every level.
BSL 1–4
Primary/secondary barriers, directional airflow, HEPA filtration, and decontamination systems integrate to contain viable organisms while maintaining sterility.
Viable counts
Microbial limits (CFU/m³) maintained through validated HVAC, pressure cascades, material transfer protocols, and real-time monitoring.