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Cronax v/s Others

Discover why OEM factory manufacturing delivers superior performance, scalability and long-term reliability compared to trading-based brands.

Comparison Parameter Cronax Industries (OEM) Typical Market Brands
Manufacturing Experience 12+ Years of Manufacturing Expertise
Since 2013
Limited or Recent Market Players
Manufacturing Model In-House OEM Manufacturing Facility
Factory Direct Supply
Dealer, Reseller, Importer or Assembly-Based Supply
Pass Boxes Configuration Manufactured in Dynamic & Static Variants with Custom Size Options Limited & Standard Configurations Only
Material & Construction SS 304 / SS 316 / Powder-Coated MS
Cleanroom-Grade Construction
Limited Material Options
Air Velocity & Filtration Design Engineered High-Velocity Airflow
HEPA / Pre-Filter Integrated Design
Contamination Control
Fixed Design with Limited Engineering Optimization
Customization Capability Dimensions, Door Type, Interlocking Logic,
Control Panels & Accessories Customizable
Standard Stock Models Only
Compliance & Certifications ISO Certified Manufacturing CE, GMP & EN
Compliance, NABL Lab Tested Performance
Certified Quality
Limited or No Verified Cleanroom Certifications
Bulk & Project Fulfillment Pharma, Food, Electronics & Industrial Projects
Large Quantity Order Handling Capability
Project Ready
Limited Capacity for Large Projects
Warranty & Support Model On-Site Part Replacement Warranty with
Lifetime Customer Support
Warranty with Paid Service Charges
Limited Post-Sale Support
Spare Parts Availability Long-Term OEM Spare Parts Stock Support
Future Safe
Limited Spare Parts Availability

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Why Industry Leaders Choose Cronax Industries

Cleanroom Pass Boxes Manufacturer. A Complete Guide.

What Is a Pass Box?

A pass box (also written as passbox or pass-through box) is a critical cleanroom accessory designed to transfer materials, tools, components, or documents between two areas of different cleanliness classifications — without requiring personnel to physically enter either zone and risk contamination.

Think of it as a sealed, controlled airlock built into a wall. One door opens on the “dirty” side, materials are placed inside, and after a decontamination cycle (or simply after the first door closes), the other door opens on the “clean” side. The two doors are mechanically or electrically interlocked, meaning both can never be open simultaneously — this is the foundational principle that prevents cross-contamination. Pass boxes are indispensable wherever maintaining air quality, sterility, or particle counts is non-negotiable.

Static Pass Box:
A Static Pass Box is used to transfer materials between two non-classified or similarly classified cleanroom areas without personnel movement. It does not have an integrated airflow or filtration system, making it an economical solution for minimizing contamination during material transfer.

Dynamic Pass Box:
A Dynamic Pass Box is designed for transferring materials between areas with different cleanliness classifications. It is equipped with a HEPA-filtered airflow system that continuously flushes the chamber with clean air, effectively removing airborne contaminants before and during material transfer. This makes it ideal for pharmaceutical, biotechnology, and sterile manufacturing applications where strict contamination control is essential.

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Key Features of Cronax Pass Boxes

1. Dual-Door Interlocking System

Our proprietary interlock mechanism ensures absolute physical impossibility of both doors being open simultaneously. Available in three configurations: purely mechanical (zero power dependency), electro-mechanical (solenoid with LED indicators), and PLC-controlled (full logging and remote monitoring).


2. H14 HEPA Laminar Flow (Dynamic Models)

Industry-leading H14-class HEPA filters — not the H13 filters many competitors use — deliver 99.995% particle capture efficiency. The result is a verified ISO Class 5 environment inside the dynamic pass box chamber, qualifying your transfer process for the most demanding GMP environments.


3. UV-C Germicidal Sterilisation (Optional)

Integrated germicidal UV-C lamps (254 nm) provide active surface decontamination during the transfer cycle. The UV interlock ensures lamps are only active when both doors are sealed, protecting operators. Lamp life counter alerts maintenance teams before efficacy drops.


4. PLC Control with Data Logging (Premium Option)

Our advanced control package includes a 7-inch colour touchscreen HMI, PLC-controlled door interlocks, HEPA fan speed feedback, UV cycle timer, alarm logging, and 21 CFR Part 11-compatible audit trail for pharmaceutical facilities under FDA oversight.


5. Crevice-Free Interior Design

All internal surfaces are continuously welded with no blind spots, crevices, or dead zones. Internal corners are radiused to ≥R12mm. Removable floor grating allows complete internal access for cleaning validation. This is not just aesthetics — it is cleanability by design.


6. Tool-Free Filter Replacement

HEPA filter cartridges slide out from the top panel without tools, requiring no special training and no cleanroom shutdown during routine filter maintenance.


7. Borosilicate Viewing Window

Toughened borosilicate glass viewing windows allow visual inspection of transferred materials without opening either door. Standard size: 200mm × 200mm. Custom sizes available.


8. Visual & Audible Alarm System

LED indicators on both sides clearly show door status (open/closed), fan status, UV status, and interlock state. An optional audible alarm alerts operators if a door is left ajar or an interlock fault is detected.


9. Low-Noise EC Motor (Dynamic Models)

Electronically commutated (EC) brushless motors deliver exceptional energy efficiency, extended service life (50,000+ hours MTBF), and noise levels below 55 dB(A) — suitable for hospital and laboratory environments where acoustic comfort matters.

Pass boxes are not one-size-fits-all. Cronax engineers its product range to address the specific contamination control challenges of each industry.

1. Pharmaceutical Manufacturing

The most demanding application for pass boxes. GMP regulations (Schedule M, WHO-GMP, EU Annex 1) mandate controlled material transfer at every cleanroom boundary. Cronax pass boxes are specified for:

Tablet and capsule manufacturing (ISO Class 7/8 areas) | Sterile injectable manufacturing (ISO Class 5/6/7) | API synthesis and milling (containment applications) | Packaging material receipt and sampling | QC laboratory sample receipt


2. Biotechnology & Life Sciences

Biopharmaceutical manufacturing requires rigorous aseptic technique. Our pass boxes with UV sterilisation and HEPA laminar flow are ideal for:

Cell culture media and reagent transfer | Fermentation vessel sampling | Gene therapy and mRNA manufacturing suites | Bioreactor consumable transfer


3. Hospital Pharmacy & Sterile Compounding

Hospital sterile compounding units (SCUs) and cytotoxic drug preparation areas use Cronax pass boxes to:

Transfer IV bags and vials into BSC/isolator areas | Receive sterile supplies without personnel entry | Maintain segregation between preparation and dispensing areas


4. Semiconductor & Microelectronics

Sub-micron contamination is catastrophic in chip fabrication. Our antistatic-grounded pass boxes (with ESD dissipative interior coatings) serve:

Wafer handling transfer in ISO Class 3–5 fabs | PCB assembly cleanrooms | MEMS device manufacturing | Display panel manufacturing (TFT/OLED)


5. Research & Testing Laboratories

Microbiology and virology research labs (BSL-2, BSL-3) | Environmental testing laboratories | Food safety and quality testing labs | Material science research facilities


6. Food & Beverage Processing

High-care food production areas, ready-to-eat (RTE) facilities, and dairy product cleanrooms require the same contamination-free transfer principles as pharmaceutical plants. Cronax’s all-SS, easy-clean pass boxes meet food safety standards.


7. Battery & EV Manufacturing

Lithium-ion battery cell manufacturing requires controlled humidity and particulate environments. Cronax pass boxes designed for dry room integration (with humidity-tolerant gaskets and coatings) support the booming Indian EV manufacturing sector.

Frequently Asked Questions About Pass Boxes


Q1. What is the difference between a static and a dynamic pass box?

A static pass box relies entirely on the facility’s pressure differential to prevent contamination — it has no active air handling. A dynamic pass box incorporates an internal HEPA fan-filter unit that actively creates laminar airflow inside the chamber, purging particles from transferred items and achieving ISO Class 5 conditions. For pharmaceutical GMP and high-grade cleanrooms (ISO Class 5–7), a dynamic pass box is typically mandated. For lower-grade areas (ISO Class 7–8) or less sensitive transfers, a static pass box is sufficient and more cost-effective.


Q2. What materials are Cronax pass boxes made from?

The standard construction uses AISI 304 stainless steel for the body and all internal surfaces, with a mirror-polished interior (Ra ≤ 0.4 µm) and satin or mirror exterior finish. For highly corrosive environments or pharmaceutical API applications requiring enhanced chemical resistance, we offer SS 316 / 316L as standard material. Mild steel with epoxy powder coating is available for non-pharmaceutical, budget-constrained applications.


Q3. Can both doors of a pass box be opened at the same time?

No — by design. The interlock system (mechanical or electro-mechanical) ensures that only one door can be opened at any given time. This is the defining safety and contamination-prevention feature of a pass box. If one door is open, the opposing door’s latch is physically or electrically disabled. Both Cronax mechanical and electro-mechanical interlocks are fail-safe: a power failure defaults to the secure (interlocked) state.


Q4. How often do HEPA filters in a dynamic pass box need replacement?

Under normal operating conditions, H14 HEPA filters in Cronax dynamic pass boxes have a typical service life of 12–24 months. The actual replacement interval depends on the particulate load of the incoming air, usage frequency, and whether pre-filters are installed. We recommend filter integrity testing (DOP/PAO challenge test) every 6 months as part of routine qualification maintenance. Cronax supplies OEM replacement filters and provides AMC support.


Q5. What cleanroom class is achieved inside a Cronax dynamic pass box?

Cronax dynamic pass boxes with H14 HEPA filtration achieve ISO Class 5 (Federal Standard 209E: Class 100) conditions inside the chamber during the laminar flow cycle, measured at ≥0.5 µm particle size. This is verified by particle count testing per ISO 14644-1 and is documented in our factory test report supplied with every unit.


Q6. Do you provide IQ/OQ documentation for pharmaceutical clients?

Yes. Cronax provides a comprehensive qualification document package including:

  • Factory Acceptance Test (FAT) report
  • Installation Qualification (IQ) protocol and report template
  • Operational Qualification (OQ) protocol and report template
  • HEPA filter integrity test certificate (PAO challenge)
  • Calibration certificates for measuring instruments used
  • User manual and maintenance schedule

These documents are formatted to support regulatory submissions to CDSCO, WHO-GMP inspectors, USFDA, MHRA, and other global regulatory bodies.


Q7. What wall thickness can Cronax pass boxes be installed in?

Standard Cronax pass boxes accommodate wall thicknesses between 100 mm and 350 mm. For thicker walls or special installations (double-wall sandwich panel systems, glass-reinforced plastic cleanroom panels), we manufacture custom extension frames. Provide your wall construction details during enquiry and our team will engineer the correct mounting solution.


Q8. Can the pass box size be customised for large components?

Absolutely. Customisation is a core capability at Cronax. We engineer pass boxes to accommodate items ranging from small vials and petri dishes to large trays, drums, and equipment components. Provide your largest transfer item’s dimensions and our engineers will design the optimal internal chamber size, ensuring the item can be transferred with clearance and that the HEPA airflow pattern (in dynamic units) covers the load effectively.


Q9. Is an electrical connection required for a static pass box?

Not necessarily. Static pass boxes with purely mechanical interlocks require no electrical connection and are fully operational in any facility, including areas with no convenient power outlet nearby. If you require LED status indicators or an electro-mechanical interlock, a 220V AC connection is needed. Dynamic pass boxes always require a power connection for the HEPA fan motor.


Q10. What is the typical delivery time for a Cronax pass box?

Standard catalogue models are delivered within 2–3 weeks of order confirmation and advance payment. Fully customised units — special dimensions, special materials, PLC controls, or RTP ports — are delivered in 4–6 weeks. Urgent requirements can be discussed on a case-by-case basis. Contact our sales team for project-specific timelines.


Q11. Do you export pass boxes internationally?

Yes. Cronax Industries exports pass boxes to customers in the UAE, Saudi Arabia, Bangladesh, Sri Lanka, Kenya, Tanzania, Nigeria, and Southeast Asian markets. We manage export documentation, pre-shipment inspection, and can provide CE marking documentation for European market customers on request.


Q12. How do I determine the right size pass box for my application?

The determining factors are: (a) the largest item you will transfer, (b) your wall construction and available cutout dimensions, and (c) the cleanroom classification on both sides of the wall. Contact Cronax with these three pieces of information and we will recommend the right model. We also offer free facility assessments for large projects.

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