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VHP (Sterilizing) Pass Box Supplier for Pharmaceutical Cleanrooms

VHP (Sterilizing) Pass Box Supplier for Pharmaceutical Cleanrooms

High-containment pharmaceutical processes require reliable surface bio-decontamination before raw materials and components enter Grade A/B sterile suites. As a dedicated VHP (Sterilizing) pass box supplier for pharmaceutical cleanrooms, Farclean manufactures automated vaporized hydrogen peroxide decontamination chambers engineered to achieve a 6-log sporicidal reduction without compromising production efficiency.

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Advanced Bio-Decontamination Cycle Engineering

Farclean VHP pass boxes integrate state-of-the-art sterilizer control systems and tight pressure seals to guarantee safe, repeatable, and fully validated bio-decontamination cycles:

  • Airtight Inflatable Gasket Doors: Pneumatic inflatable silicone door seals prevent VHP gas leakage during exposure phases, guaranteeing zero chemical release into surrounding cleanroom corridors.
  • Integrated VHP Generator Options: Available with fully integrated internal VHP generators or customized connection ports for central facility VHP loop systems.
  • Four-Phase Automated Cycle: Fully automated sequences managing Dehumidification, Conditioning, Sterilization (VHP injection), and Aeration phases via PLC automation.
  • Rapid Catalytic Aeration: High-efficiency catalytic converters break down residual H2O2 vapor into harmless water vapor and oxygen, drastically reducing cycle turnaround times.
  • 316L Stainless Steel Chamber: High-grade 316L interior wall panels with electropolished finishes ensure maximum resistance to continuous oxidizing sterilants.

VHP Pass Box Performance Parameters

System Parameter Technical Specification Pharmaceutical Compliance Standard
Bio-Decontamination Level 6-log kill reduction (Geobacillus stearothermophilus) Complies with EU GMP Annex 1 & FDA sterile processing guidelines.
Sealing Mechanism Inflatable pneumatic gaskets with pressure monitoring Guarantees Class 1 gas-tight containment during sterilization.
Control Architecture Siemens PLC with color HMI touchscreen & audit trail logging Fully compliant with 21 CFR Part 11 electronic record requirements.

Full Validation Support (DQ/IQ/OQ/PQ)

Farclean supplies complete validation documentation packages and FAT/SAT testing support to streamline your facility’s qualification process. Contact our engineering specialists today to design a VHP transfer solution tailored to your sterile facility layout.

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