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.
Melbourne is the centre of Australian pharmaceutical manufacturing, from the Parkville biomedical precinct to large-scale biologics and vaccine plants. We provide pharmaceutical HVAC and cleanroom precision cooling for Melbourne sites and validated environments nationwide, with ARC-licensed technicians and service reports formatted for GMP and TGA validation files.
Typical configurations
CRAC patterns
we deploy
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.
Related services
CRAC services for Pharmaceutical & Cleanroom
Locations
Where we serve Pharmaceutical & Cleanroom
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