Dry rooms at PES Pharma are engineered where humidity defines feasibility. We deliver environments maintaining dew points down to -40°C and relative humidity below 1% critical for moisture-sensitive pharmaceutical processes and beyond.

Technical Criteria:

Dew point control: -40°C (or lower where required)

Relative humidity: <1% through multi-stage desiccant systems

Temperature stability: ±0.5°C with redundant HVAC control

ISO-compliant cleanroom integration (ISO 5–8 as required)

Applications:

Hygroscopic API handling and powder processing

Moisture-sensitive granulation and blending

Dry powder inhalation product manufacturing

Lithium-ion battery electrode and electrolyte production—where moisture exposure compromises performance and safety

Operational Integration:

Material transfer systems, utility connections, and personnel access maintain environmental integrity throughout operations. Real-time monitoring alerts to any deviation, ensuring conditions remain within validated parameters. PES Pharma translates pharmaceutical-grade precision into industries where moisture control determines product viability from life sciences to advanced energy storage.