Industry
Cleanroom & Validated Cooling for Pharma | Australia
Pharmaceutical cleanrooms require tight temperature, humidity, and particulate control to ISO 14644 cleanliness classes. CRAC Services delivers HVAC and precision cooling for vaccine manufacturing, biologics, sterile fill-finish, and analytical labs across Australia, with GMP-grade documentation.
Typical configurations
CRAC patterns
we deploy
Cleanroom AHU + HEPA
Validated CRAC with documented IQ/OQ/PQ
Cold-chain precision cooling (-80°C through ambient)
Humidity-controlled environments (RH ±5%)
Considerations
Key considerations for Pharmaceutical & Cleanroom
01
Validation packs
GMP environments require IQ/OQ/PQ documentation and change-controlled work. Our service reports are formatted to drop into validation files.
02
Cold chain
Vaccine and biologics storage at -80°C cannot tolerate brief outages — cooling redundancy is critical.
03
Humidity control
Many pharma processes are humidity-sensitive — RH must be controlled within ±5% in validated rooms.
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