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Malaysia 126 m² PAC Biopharmaceutical Cleanroom

Completed in Malaysia in 2024, this 126 m² PAC cleanroom provides an ISO 8 environment for biopharmaceutical applications.

Completed in Malaysia in 2024, this 126 m² PAC project provided an ISO 8 environment for biopharmaceutical operations. The client required clean space that could be prepared as modules and installed quickly after delivery. A prefabricated cleanroom configuration was chosen, with the walls, ceiling, HVAC, filtration, lighting, electrical services, automation, and monitoring coordinated as one package. The cleanroom wall panels formed part of the pre-assembled enclosure, while module installation, commissioning, and validation completed the site scope. The recorded lead time was two months. This modular cleanroom example shows how PAC delivery can suit a mid-sized controlled area where transport and on-site connections can be planned in advance. The published case does not identify the client or give process-specific equipment details. It also does not claim measured performance beyond the ISO 8 classification stated in the project information.

Malaysia 126 m² PAC Biopharmaceutical Cleanroom
126 m² Controlled area
2 months Delivery
ISO 8 Cleanroom class
01
THE CHALLENGE

Working Around Real Project Constraints

Create approximately 126 m² of ISO 8 biopharmaceutical clean space with pre-assembled modular delivery and rapid site installation.

02
THE SOLUTION

Engineered for the Process

Pre-assembled PAC cleanroom modules provided 126 m² of ISO 8 space for biopharmaceutical use in Malaysia.

SCOPE OF DELIVERY

A Coordinated Cleanroom Package

The project package was coordinated as a complete system, keeping architectural, mechanical and controls interfaces aligned from design through qualification.

  • 01Pre-assembled modular walls and ceiling for a 126 m² biopharmaceutical cleanroom
  • 02HVAC and filtration serving the ISO 8 clean space
  • 03Lighting, electrical, automation and monitoring systems
  • 04On-site module installation, commissioning and validation
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