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WONCLEAN Cleanroom Systerm
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Clean rooms and modular laboratories are two common experimental environments in scientific research....
Modular clean room
Modular clean room
Modular Clean Rooms & Prefab Laboratories — Factory-Built, Fast to Deploy A modular clean room is a factory-built, prefabricated controlled environment assembled from standardized wall, ceiling and HVAC components — delivering ISO 14644 / GMP-grade cleanliness in weeks instead of months. As a turnkey modular cleanroom manufacturer since 2005, Wonclean designs, produces and installs flexible, expandable and relocatable systems for pharmaceutical, biotech, electronics, medical and laboratory projects worldwide. Explore our modular solutions: Modular Clean Room Prefabricated Laboratory Container Laboratory Folding Laboratory Each room is built from our own wall and ceiling systems, so quality and lead time stay under one roof. Tell us your target ISO/GMP class, area and layout — get a free layout & quote within 24 hours.
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Clean room wall system
Clean room wall system
Clean Room Wall Systems — Flush, Demountable Partition & Panel Solutions A clean room wall system is the flush, airtight envelope that defines a controlled environment — sandwich panels, demountable partitions and matching corner, skirting and joint profiles that leave no dust-collecting ledges. Built to a ≤ 2 mm/2 m flatness tolerance, Wonclean wall systems are fully demountable, so panels can be modified or relocated without disturbing adjacent panels or the ceiling — ideal for pharmaceutical, electronics, food and laboratory cleanrooms. Browse the wall system range: Sandwich Panel HPL Sandwich Panel Medical Cleanroom Panel Demountable Partition Wall Partition System Injection Panel Choose your panel core — fire-rated, insulated or chemical-resistant — from our cleanroom panel range, paired with matching doors and windows. Send us your wall layout and ISO/GMP class — get a free quote within 24 hours.
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Clean room ceiling system
Clean room ceiling system
Clean room ceiling system is an important part of the clean room system. It consists of an aluminum alloy t grid system and a ceiling system. It is usually used in clean room projects where the cleanliness level is relatively high, for example: Class 100, Class 1000, 100000 It is widely used in the electronics industry, chemical industry, military industry, etc., and it is also used in other industries. The main function of the Clean room ceiling system is to support FFU (Fan, Filter Unit) equipment, fire sprinkler systems, lighting systems, broadcasting systems, etc. The Clean room ceiling system is suspended from the building structure or steel structure by suspension components. The Clean room ceiling system produced by our company has been carefully designed and developed over 10 years, combined with the advantages of various T grid systems, with light weight, high strength, walkable, easy to install, and so on. It is the basis for multiple system installations.
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Clean room door&windows
Clean room door&windows
Manufacturingclean room doors include HPL door、stainless steel door、steel door and glass door etc . According to the switch mode of the door, it can be divided into pull/push door and sliding door.Our clean room doors are compatible with any level of clean room and can be customized to your needs. We use high quality steel to make the door and double seal on all sides to prevent leakage and contamination. We offer features such as custom sizes and colors, electronic locks and cleaning strips. The clean room window we produced, consists of two categories: single-glazed glass window and double-glazed window. The single-layer glass window features high transparency, low price, simple structure and easy installation. The double-glazed window is characterized by insulation. good thermal insulation, high transparency, beautiful appearance and so on. We will inject dry air or nitrogen into the double-glazed window, and a desiccant will be placed in the frame of the window to ensure that no water vapor will appear in the double-glazed window.....
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Clean room equipment
Clean room equipment
There are many types of clean room equipment, including ventilation equipment, lighting equipment, fire fighting equipment, electrical equipment, etc. There are four  kinds of clean room equipment produced by our company, pass box、air shower、Purified laminar flow cover andweighing cover.There are widely usedin the clean room system. Pass Box The pass box is widely used in LCD, electronic factory, micro technology, biological laboratory, pharmaceutical factory, hospital, food processing industry and other places that need air purification.The main function of the Pass box is to transfer items, reduce the movement of people in the clean room to reduce the generation of dust, and also act as a small item transfer. Air shower The air shower has a series of air shower for people, and a series of air shower for goods.There are various combinations of blowing showers such as single-side blowing showers, double-side blowing showers, and top blowing showers; air shower doors include manual doors, automatic doors, and fast rolling shutter doors.The air shower is the passage that a person must pass through when entering the clean room. It uses the high-speed air to blow the personnel to eliminate the dust particles brought into the clean room and ensure the cleanliness of the room....
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Cleanroom Panel
Cleanroom Panel
Cleanroom Panels — Wall & Ceiling Sandwich Panels for Controlled Environments A cleanroom panel is the core building block of pharmaceutical, biotech, electronics, food and laboratory facilities — a sandwich panel that forms airtight, dust-free walls, ceilings and partitions. As a cleanroom panel manufacturer since 2005, Wonclean engineers every board to a ≤ 2 mm/2 m flatness tolerance, with the fire rating, insulation, moisture resistance and surface you need — all from a single supplier shipping to 40+ countries. The difference between panels is the core and facing. Browse the full range by type: MgO Rock Wool Rock Wool Silica Rock Aluminum Honeycomb HPL PU PIR Insulated Duct Not sure which core fits your fire, insulation or budget needs? Tell us your project and our engineers will recommend the right panel and send a free quotation within 24 hours.
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    Established

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About us
WONCLEAN COMPANY LIMITED
Established in 2005，WONCLEAN COMPANY LIMITED is a leading provider of modular laboratory and cleanroom systems for the pharmaceutical, medical devices, food, and electronics industries. We specialize in delivering cutting-edge solutions encompassing modular laboratories, cleanrooms, wall panels, ceiling panels, HPL sandwich panels, lighting systems, HVAC system materials, and equipment. Our product range is designed to meet stringent industry standards and requirements, ensuring high-performance and reliability throughout various cleanroom envi...
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Our factory
What makes a 20-year source factory the best choice for your 2026 sterile facility? Explore our factory’s direct manufacturing power, offering comprehensive cleanroom systems without middleman costs.

20 Years of Direct Manufacturing Excellence in Cleanroom Systems

What defines a true industry leader? Since 2005, our factory has stood as a cornerstone of sterile infrastructure. We are not a middleman or a trading company; we are a direct source manufacturer with two decades of deep-rooted expertise. By controlling the entire production chain—from raw material processing to final assembly of cleanroom panels and ceiling grids—we ensure unmatched quality and factory-direct pricing for 2026 global modular projects.

1. What is the foundation of our factory's 20-year legacy?

For 20 years, our factory has been the silent engine behind 500+ successful sterile environments. As a technology-driven manufacturing group, we specialize in the R&D of high-pressure laminate (HPL) and modular systems. Our longevity is a testament to our commitment to quality, ensuring that every panel and grid meets the 2026 ISO 14644 and GMP standards. Unlike distributors, we own every machine and every patent.

our factory's 20-year manufacturing base and R&D center 2026

2. How does our factory eliminate middlemen to maximize your ROI?

In 2026, cost-efficiency and transparency are paramount. Unlike traditional trading brands, our factory manages the complete lifecycle of cleanroom components. This "Source-to-Site" model ensures that you receive the highest industrial grade materials without the markup of intermediaries, while maintaining total control over precision and delivery timelines.

Comparison Pillar Our factory (Source) Middlemen / Trading Brands
Direct Factory Price Yes (No Markup) No (15-30% Commissions)
Quality Supervision Internal 24/7 Control External reliance
Lead Time Prioritized Scheduling Delayed by coordination
Technical Support Direct Engineer Access Sales-level only

3. What range of products does our factory manufacture?

We provide full-range coverage of cleanroom solutions. our factory produces everything under one roof: from heavy-duty HPL sandwich panels and walkable ceiling grids to integrated LED lighting and specialized HVAC equipment. Whether it's a modular laboratory or a large-scale electronic cleanroom, we cover every component needed for a fully functional ISO-certified facility.

Comprehensive cleanroom product range manufactured in our factory

4. Which advanced technologies power our factory's lines?

Precision is the soul of our factory. We utilize 3D-BIM space technology to synchronize our manufacturing lines with your design requirements. Because we own the processes, we can guarantee that every modular component for pharmaceutical or semiconductor labs fits with sub-millimeter accuracy. Our strategic bases in China and Malaysia ensure global delivery within days.

our factory global industrial layout and precision manufacturing scale

5. What specialized industries do we serve directly?

With 20 years of data, our factory specializes in high-standard solutions for the Biopharmaceutical, Electronic Semiconductor, New Energy, and Cosmetics sectors. Our materials are specifically engineered to target ESD control, chemical resistance, and Class A1 fire safety, meeting the most rigorous 2026 GMP hygiene requirements.

6. How do we guarantee long-term after-sales excellence?

Being a source factory means we are here for the long haul. our factory service commitment includes a 2-year warranty on modular equipment and a 24-hour rapid response system. Because we are the manufacturer, spare parts and modification components are always in stock, protecting your investment and ensuring facility flexibility.

Expert FAQ: Strategic Factory Solutions

What does "Source Factory" mean for my project? It means you buy directly from the creator. This eliminates middleman fees, ensures 100% quality traceability, and gives you direct access to the engineers in our factory.
How do you ensure the durability of your panels? We utilize HPL produced under 1400 PSI and aluminum honeycomb cores that resist impact and corrosion for over 15 years.
Which certifications does our factory hold? Our systems are engineered to meet ISO 14644, GMP, and Class A1 fire safety standards, backed by numerous technical patents.
Honor certificates
  • License Verified Report
  • 稳众洁净科技有限公司获 ISO9001:2015 认证 — 高品质特殊设备制造专家
  • Certificate Of Registration 1
  • Design Patent Certificate
  • SGS certification
  • SGS certificates
  • SGS certificates
  • Business License

Company profile

Our factory

Honor certificates
Company profile
About us
Established in 2005，WONCLEAN COMPANY LIMITED is a leading provider of modular laboratory and cleanroom systems for the pharmaceutical, medical devices, food, and electronics industries. We specialize in delivering cutting-edge solutions encompassing modular laboratories, cleanrooms, wall panels, ceiling panels, HPL sandwich panels, lighting systems, HVAC system materials, and equipment. Our product range is designed to meet stringent industry standards and requirements, ensuring high-performance and reliability throughout various cleanroom envi...
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Our advantage
The trustworthy global enterprise in the field of Cleanroom&Modular laboratory system
  • Planning and design
    Planning and design
    Expert Process-Driven Planning From project initiation, we collaborate closely with clients to conduct scientific plant layout planning and functional zoning, ensuring that spatial arrangement aligns precisely with production processes to enhance operational efficiency. Industry-Tailored Technical Design Leveraging years of integrated design and co...
  • Produce
    Produce
    The quality of the product is not tested, but produced. Professionalism comes from  concentration. We have been designing and manufacturing in the clean room industry for 15 years. Through Years of working and production experience，we have realized that only continuous learning, innovation, and can keep up with the progress of the industry.
  • Install
    Install
    Since 2005, we have had a lot of on-site installation experience in mainland China and overseas markets. In these experiences, we are constantly improving our construction technology level, and we have cultivated many excellent technical installers.  The quality, progress and safety of the project can be effectively controlled to ensure the sm...
  • After sale
    After sale
    Reliable Warranty & Timely Support Wonclean Technology provides customers with comprehensive, guaranteed, and all-round after-sales service. We offer a 3-year warranty for quality problems on modular cleanroom equipment and components, ensuring your investment is protected. Our commitment is further backed by professional after-sales teams who ...
Application fields
Building program and service for information electronics, Pharmaceuticals, food,cosmetics, military industry, chemical industry and etc...
News&Events
News&Events
Full display of the latest company news and shipping news
Modular Clean Labs for Medical Device Manufacturing: Planning ISO Class, ACH and Clean Zones
08-03

2026

Modular Clean Labs for Medical Device Manufacturing: Planning ISO Class, ACH and Clean Zones

Technical Planning Guide | Medical Device Clean Lab Modular Clean Labs for Medical Device Manufacturing: Planning ISO Class, ACH and Clean Zones Medical device manufacturing often needs a controlled clean lab that is smaller, faster and more flexible than a full conventional plant. A modular clean lab can support pilot production, assembly, inspection, packaging or process development, but only when ISO class, airflow, ACH assumptions and clean-zone boundaries are planned as one technical system. modular clean lab medical device cleanroom ISO cleanroom class ACH and airflow ISO ClassDefine the required airborne particle limit and occupancy state. ACHUse air changes to size airflow, not to prove cleanliness alone. ZonesSeparate assembly, inspection, transfer and support areas. QMSKeep layout evidence aligned with device quality records. For medical device teams, the best modular clean lab is not simply a container with clean panels. It is a controlled space where product exposure, operator movement, particle sources, material transfer, cleaning method and quality documentation all point to the same risk-based design. Modular clean lab deployment. Exterior speed is useful only when the internal clean zones, HVAC access and transfer routes are designed for the device manufacturing process. Risk-Based Planning Start with the Device Process, Not the Container Size A modular clean lab for medical devices should begin with the device and the process: is the product open or packaged, dry or wet, sterile or non-sterile, implantable or external use, manually assembled or automated, inspected in-process or at final packaging? Each answer changes the clean-zone logic. ISO 13485:2016 is the international quality management system standard for medical devices. It does not prescribe a cleanroom layout, but it reinforces the need for controlled production conditions, documented processes and risk-based quality planning. A clean lab layout should therefore be easy to explain in the device manufacturer's quality file. For early design, define the product exposure steps, personnel count, equipment heat load, material entry, waste exit, cleaning method, monitoring points and batch or lot documentation before fixing the module footprint. ISO Class and ACH ISO Class Is Verified by Particles; ACH Is Only One Design Input ISO 14644-1 classifies cleanrooms by airborne particle concentration. ACH can help estimate airflow volume, but it cannot prove ISO class by itself. A clean lab with high ACH can still perform poorly if return paths are blocked, operators create uncontrolled turbulence, filters leak or workbenches sit in dead zones. ISO 14644-3 covers cleanroom test methods, including checks that help confirm airflow, pressure difference and installed filter system performance where specified. For modular clean labs, the design should make these checks practical after installation, not hidden behind inaccessible equipment panels. Clean lab planning points that connect ...

  • 08-03

    2026

    Pharmaceutical Cleanroom Wall Panel Design: Chemical Resistance, Flush Joints and Microbial Risk Control

    Technical Design Guide | Pharmaceutical Cleanroom Wall System Pharmaceutical Cleanroom Wall Panel Design: Chemical Resistance, Flush Joints and Microbial Risk Control Pharmaceutical cleanroom wall panels are not selected by color or panel thickness alone. The wall system must survive cleaning chemistry, limit particle shedding, reduce microbial harborages, protect pressure boundaries and keep doors, windows and utility penetrations cleanable through years of operation. pharmaceutical cleanroom wall panels chemical resistant wall panels cleanroom door interface GMP modular cleanroom ChemistryMatch panels to cleaning agents and exposure time. Flush JointsControl crevices, ledges and exposed fasteners. InterfacesSeal doors, windows, pass boxes and utilities. RiskSupport contamination control and inspection. In a pharmaceutical facility, the cleanroom wall is both an architectural surface and a contamination-control boundary. It separates process rooms, supports pressure cascade, receives repeated wipe-down, carries observation windows and absorbs the abuse of carts, gowning flow and maintenance access. Cleanable wall panel corridor. Large, smooth wall fields reduce cleaning complexity, but doors, glazing, coving and service details still decide the contamination-control quality of the room. Material Selection Chemical Resistance Must Be Matched to the Actual Cleaning Program A wall panel described as chemical resistant is not automatically suitable for every pharmaceutical room. The correct review starts with the cleaning and disinfection matrix: alcohols, hydrogen peroxide, quaternary ammonium compounds, sporicides, hypochlorite, acidic detergents, alkaline detergents, contact time, wipe frequency and residue behavior. For coated steel, HPL, stainless steel or other cleanroom wall finishes, the important failure modes include discoloration, blistering, loss of gloss, softening, edge swelling, corrosion, delamination and sealant breakdown. ASTM D543 is commonly referenced for evaluating plastic material resistance to chemical reagents, while ASTM D1308 addresses the effect of chemicals on clear and pigmented organic finishes. These standards do not replace project-specific acceptance criteria, but they help buyers ask for test evidence instead of relying on broad claims. Wonclean wall panel selection should therefore be reviewed against the user's cleaning SOP, room classification, microbial control target, impact risk and expected lifecycle. A panel that performs well in a low-cleaning utility corridor may not be the right finish beside a wash-down, disinfection or sterile support process. Design Checklist A Wall Panel Specification Should Control More Than the Panel Core Key design points for pharmaceutical cleanroom wall panels. Design point Technical risk Recommended control Surface finish Residue retention, particle shedding or cleaning damage. Review coating, HPL or stainless finish against cleaning agents and wipe method. Joint geometry Crevi...

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  • 07-27

    2026

    GMP Modular Cleanroom Design for Pharma: ISO 7/8, Pressure Differential and Validation Readiness

    Technical Design Guide | Pharma GMP Cleanroom GMP Modular Cleanroom Design for Pharma: ISO 7/8, Pressure Differential and Validation Readiness A GMP modular cleanroom for pharmaceutical production must do more than achieve a target ISO 7 or ISO 8 particle class. It must support contamination control strategy, pressure differential, personnel and material flow, cleanable surfaces, monitoring access and documented validation from design through qualification. GMP modular cleanroom ISO 7 cleanroom pharmaceutical cleanroom cleanable wall panel ISO 7/8Classify particles under defined operating states. PressureProtect clean zones with a documented cascade. CCSSupport contamination control strategy. ValidationPrepare DQ, IQ and OQ evidence early. In pharmaceutical facilities, modular cleanroom design must balance speed with evidence. A factory-built or modularized envelope is valuable only when its surfaces, joints, airlocks, doors, HVAC interfaces and monitoring points can be documented and verified against GMP expectations. GMP corridor and room interfaces. Doors, windows and ceiling returns should support pressure differential and cleanable room boundaries. GMP Design Logic Start with Contamination Control, Not Only Room Class A pharmaceutical cleanroom should be designed from process risk: open product exposure, microbial risk, personnel intervention, material transfer, cleaning frequency, equipment maintenance and environmental monitoring. ISO 7 or ISO 8 targets are important, but they are only one part of the contamination-control picture. EU GMP Annex 1 emphasizes a contamination control strategy for sterile product manufacturing. Even when a room is not Grade A/B, the modular cleanroom envelope should help control contamination routes through cleanable construction, pressure control and defined flows. Wonclean modular cleanroom projects should therefore be reviewed with user requirement specifications, process flow diagrams, HVAC zoning, panel elevations, door interlocks and qualification documents before production starts. ISO 7/8 and Pressure ISO 7/8 Rooms Still Need a Real Pressure Differential Strategy ISO 14644-1 classifies cleanrooms by airborne particle concentration. In GMP facilities, the same room also needs a defensible pressure differential strategy that reflects product protection, cross-contamination risk, personnel movement and material transfer. A modular envelope can make pressure control easier because wall panels, doors, windows and penetrations are repeatable. But the design must avoid uncontrolled leakage. Door gaps, pass-through seals, ceiling returns and utility penetrations can all weaken a pressure cascade. Validation-ready design checks for GMP modular cleanrooms. Design item GMP risk Evidence to prepare Pressure cascade Cross-contamination or loss of product protection. Room pressure map, alarm logic and balancing report. Airlock sequence Personnel or material flow can bypass control points. Door interlock logic and op...

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  • 07-27

    2026

    Selecting Semiconductor Cleanroom Ceiling Systems: T-Bar Ceiling, FFU Coverage and ISO Cleanliness Control

    Technical Analysis | Semiconductor Cleanroom Ceilings Selecting Semiconductor Cleanroom Ceiling Systems: T-Bar Ceiling, FFU Coverage and ISO Cleanliness Control In a semiconductor cleanroom, the ceiling is the air delivery platform, service layer and structural interface for FFUs, filters, lighting, access panels and monitoring points. A T-bar ceiling system must therefore be selected around ISO cleanliness targets, FFU coverage, leakage control and maintenance access, not only profile dimensions. T-bar ceiling cleanroom ceiling FFU ceiling fan filter unit GridCarry FFUs, lights, panels and access loads. CoverageMatch airflow pattern to ISO class and heat load. SealControl bypass leakage at filters and ceiling joints. ServiceEnable safe filter, FFU, cable and lighting maintenance. The wrong ceiling choice can make a cleanroom expensive to qualify and painful to maintain. FFU density may look sufficient on a plan, but if the ceiling grid deflects, filters are difficult to change, gasket details leak or returns are poorly placed, the room may struggle to meet ISO classification and recovery expectations. T-bar profile and sealing logic. The ceiling grid must locate, support and seal FFUs, lights, blank panels and access modules with repeatable precision. Selection Logic Start with the ISO Target, Then Build the Ceiling Around Airflow ISO 14644-1 defines airborne particle cleanliness classes, but it does not prescribe a single ceiling construction. The ceiling designer must translate the target class into air supply strategy, filter location, return-air path, recovery expectation and maintenance access. For semiconductor rooms, ceiling design should also account for tool heat, equipment height, process sensitivity, AMC strategy, static-control needs and above-ceiling service traffic. A ceiling that works for a small metrology lab may be inadequate for a dense process bay with frequent filter service and strict pressure control. Ceiling as airflow platform. Light positions, diffuser or filter locations and blank panels should support clean airflow instead of fighting it. FFU Coverage FFU Coverage Is a Performance Decision, Not a Marketing Percentage FFU coverage is often discussed as a percentage of ceiling area, but the useful question is whether clean air reaches the risk locations and returns without short-circuiting. A high coverage number can still perform poorly if FFUs are clustered away from tools, blocked by equipment, mixed with poorly sealed blank panels or not balanced with returns. The project team should define air velocity targets, filter module size, control zones, redundancy, energy strategy and filter replacement sequence. For particle-sensitive semiconductor spaces, HEPA or ULPA filter class and documentation should be aligned with a recognized filter framework such as ISO 29463-1. FFU ceiling decisions that affect ISO cleanliness control. Decision Why it matters Practical check FFU density Controls supply volume, recovery and loca...

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Case Center
We have  cooperated with many well-known domestic pharmaceutical companies, R&D centers, hospitals, and disease control centers. Established long-term cooperative relationship. These include Qilu Pharmaceutical, Wanhua Chemical, Luye Pharmaceutical, Kanghong Pharmaceutical, Shanghai Fudan University, Shenzhen Nanshan Hospital, Shenzhen Pin...
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