Core building blocks are delivered entirely in-house: modular panels, airtight doors, flush glazing, hygienic coving, multistage HEPA/ULPA filtration, and purpose-engineered HVAC. Utilities—WFI, pure steam, process gases, compressed air, electrical, and EMS/BMS—are integrated and pre-coordinated, ensuring balanced startup and full traceability.

GMP-controlled installation, followed by commissioning and IQ/OQ/PQ, provides documented verification of pressure stability, HEPA efficiency, microbial control, and water-system compliance—delivering a fully auditable and stable operating environment tailored for sterile and aseptic processing.

Our engineering approach is built around process-first facility design, ensuring every cleanroom, utility line, and interface point directly supports your technology node and tool plan. From ISO 3–6 zoning and airflow logic to vibration/EMI control and high-purity utilities, each system is engineered for precision and scalability. This early-stage discipline eliminates redesign cycles, prevents tool-fit conflicts, and secures a facility infrastructure that protects yield from day one.

Execution is driven by precision construction and verified commissioning, where engineered intent is realized through contamination-controlled installation and synchronized tool-utility integration. Comprehensive commissioning—airflow stability, UPW quality, particle performance, vibration mapping, and interlock testing—ensures the cleanroom is fully certified before tool move-in. The result is a fab environment that is stable from the moment it opens, reducing time to yield and extending long-term production reliability.

Our design and process integration phase goes beyond layout and airflow. We map your material flow, personnel movement, and cleaning protocols to create zoned contamination barriers, allergen segregation systems, and hygienic surfaces that are fully CIP/SIP compatible. Utilities, including high-purity water, chilled water, clean steam, and air, are engineered to match your exact process demands. By planning tool interfaces, equipment placements, and sanitation access early, we prevent cross-contamination risks, reduce downtime, and enable scalable production—from low-volume specialty foods to high-throughput industrial lines.

During construction and validation, we bring the design to life under strict contamination control. Walls, flooring, and equipment are installed with clean-in-place standards in mind, airflow and pressure cascades are fine-tuned to prevent cross-zone contamination, and rigorous commissioning verifies particle counts, microbial limits, temperature, and humidity across all zones. Every facility is production-ready at handover, reducing time to market, protecting brand reputation, and ensuring consistent quality. Unlike generic solutions, Line-Link™ combines deep food-process expertise, fully customized cleanroom engineering, and integrated project delivery—so clients get a facility built exactly for their product and operational needs.