This October, CPHI Milan 2026 returns to Fiera Milano, Italy - the global premier networking hub where pharmaceutical manufacturers, engineering specialists and technology providers connect to shape the future of pharma.

At Booth 9A26, Line-Link^® is about to showcase its latest advancements in contamination control- VHP Pass Box solutions designed for different material-transfer and decontamination requirements. With in-house manufacturing, Line-Link^® integrates VHP decontamination, high-efficiency filtration, process monitoring and configurable system design for pharmaceutical and other controlled environments.

Two VHP Pass Box Types: What Is Common - and What Is Different?

Line-Link^® designs VHP Pass Boxes with the full operating lifecycle in mind. Exhaust, residue removal, control requirements, maintenance access, catalyst replacement and consumable costs are considered from the beginning - helping avoid costly facility changes and making the equipment practical to operate and maintain over time. Across both configurations, the operating fundamentals remain the same: a controlled VHP cycle, door interlocking, controlled airflow, HEPA filtration, cycle control and H₂O₂ residue management for reliable material decontamination in GMP-controlled environments.

The goal is straightforward: a VHP Pass Box that validates reliably, integrates cleanly into the facility and remains practical and economical to operate throughout its service life.

① Standard VHP Pass Box

Standard VHP Pass Box focuses on providing a practical and controlled VHP decontamination process for material transfer. Its priority is straightforward: introduce VHP, maintain the required exposure conditions, remove or reduce residual H₂O₂, and release the material once the cycle is complete.

② VHP Comprehensive Sterilization Pass Box

VHP Comprehensive Sterilization Pass Box takes this concept further by integrating several functions into one system. In addition to VHP generation and HEPA filtration, it combines a UV lamp and catalytic converter. The catalytic converter helps break down residual hydrogen peroxide into water and oxygen, providing an additional approach to residue removal after the decontamination cycle.

Which Configuration Fits the Process?

If the primary requirement is reliable VHP decontamination for routine material transfer, a conventional VHP Pass Box may provide the right balance of functionality, practicality and cost. Where the process calls for more comprehensive decontamination and integrated residual H₂O₂ management, the VHP Comprehensive Sterilization Pass Box offers a more complete equipment configuration. In both cases, the fundamentals remain the same: a controlled VHP cycle, cleanroom-compatible airflow, reliable interlocking and repeatable decontamination performance. What changes is how far the equipment goes in integrating the functions needed around that cycle. .

 About Line-Link^® 

Established in 2003, Line-Link^® has evolved into a global provider of turnkey cleanroom solutions integrating engineering, manufacturing, and project delivery within a unified operating model. Serving pharmaceuticals, biotechnology, semiconductors, healthcare, cosmetics, food production, and laboratory sectors, Line-Link^® operates as a full-scope EPC cleanroom partner with comprehensive in-house manufacturing capabilities. With advanced production facilities and engineering infrastructure, Line-Link^® maintains strict control over product quality, compliance, and system performance. Its portfolio includes cleanroom panels, doors and windows, filtration systems, pass boxes, laminar airflow units, weighing booths, air showers, stainless steel furniture, and cleanroom accessories. Supported by tailored design-build services and technical support, Line-Link^® continues delivering reliable cleanroom environments for regulated industries worldwide.

The company operates across pharmaceutical, biotech, healthcare, electronics, cosmetics, and food industries, delivering cleanroom projects from system design and manufacturing to installation and commissioning. All key products are developed under CE, ISO, and GMP-aligned standards, supported by internal production control across multiple manufacturing bases, enabling consistent quality, faster project execution, and full system compatibility.

About CPHI Milan2026

CPHI connects with thousands of industry leaders and expand your network with endless opportunities to learn, innovate, and collaborate online and in-person. CPHI facilitates opportunities for you to grow your business and develop meaningful connections at the heart of pharma.