One-Stop Turnkey Cleanroom
Solutions Provider

Intelligent Manufacturing Core, Powering a Clean Future

UPTING provides comprehensive EPC cleanroom and modular cleanroom system design solutions for companies across multiple global industries, including pharmaceuticals, biotechnology, semiconductors, electronics, medical devices, and food production. Our Intelligent Modular Cleanrooms ensure that every project delivers high quality, high energy efficiency, and scalability.

Why Choose Modular Over Traditional Construction?

Our Expertise In Cleanroom
Solutions

ISO Class 4-5 Clean Room (Class 10/100)

ISO Class 4-5 Clean Room (Class 10/100)

· Precision Micro-Environment: Utilizes FFU matrix layouts with vertical unidirectional flow. Achieves working section wind speed of 0.45±0.1m/s and controls particles down to ≥0.1μm. Ideal for lithography and wafer manufacturing.

· Precise Temp & Humidity: Equipped with constant temp/humidity units (±0.5℃ ±3%RH ) and a 4-stage filtration system (G4+F8+H13+U15) to ensure dual control of airborne particles and AMC.

· Anti-Static & Micro-Vibration: Features epoxy self-leveling floors with conductive copper mesh (10^4-10^6Ω) meeting VC-D micro-vibration standards (≤25μm/s).

ISO Class 6 Clean Room (Class 1000)

ISO Class 6 Clean Room (Class 1000)

· Precision Micro-Environment: Utilizes FFU matrix layouts with vertical unidirectional flow. Achieves working section wind speed of 0.45±0.1m/s and controls particles down to ≥0.1μm. Ideal for lithography and wafer manufacturing.

· Precise Temp & Humidity: Equipped with constant temp/humidity units (±0.5℃ ±3%RH ) and a 4-stage filtration system (G4+F8+H13+U15) to ensure dual control of airborne particles and AMC.

· Anti-Static & Micro-Vibration: Features epoxy self-leveling floors with conductive copper mesh (10^4-10^6Ω) meeting VC-D micro-vibration standards (≤25μm/s).

ISO Class 7-8 Clean Room (Class 10,000 - 100,000)

ISO Class 7-8 Clean Room (Class 10,000 - 100,000)

· Precision Micro-Environment: Utilizes FFU matrix layouts with vertical unidirectional flow. Achieves working section wind speed of 0.45±0.1m/s and controls particles down to ≥0.1μm. Ideal for lithography and wafer manufacturing.

· Precise Temp & Humidity: Equipped with constant temp/humidity units (±0.5℃ ±3%RH ) and a 4-stage filtration system (G4+F8+H13+U15) to ensure dual control of airborne particles and AMC.

· Anti-Static & Micro-Vibration: Features epoxy self-leveling floors with conductive copper mesh (10^4-10^6Ω) meeting VC-D micro-vibration standards (≤25μm/s).

Our Full-Process Delivery Workflow

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Inquiry & Discussion

Understanding your specific needs, industry standards, and site constraints.

Design & Planning

Providing 3D conceptual layouts, HVAC simulations, and comprehensive engineering drawings.

Precision Manufacturing

Manufacturing panels, doors, and core equipment at our smart factories in China and Thailand.

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Global Logistics

Flat-pack shipping ensuring safe and cost-effective delivery.

On-Site Assembly

Rapid plug-and-play installation guided by our elite engineering team.

Commissioning & Validation

Designed to support ISO, FDA and GMP validation requirements before handover.

Ready to Build Your Ideal Factory?

Contact our engineering experts today for a free consultation and a tailored 3D cleanroom design.

In-House Manufactured Equipment

Frequently Asked Questions

How long does it take to install a modular cleanroom?

Installation times vary based on size and complexity, but our pre-engineered modular systems typically reduce on-site assembly time by up to 50% compared to traditional construction methods.

Absolutely. Our “Clean Cube” system is designed with up to 90% material reusability, allowing you to easily add modules, change layouts, or move the entire structure to a new facility.
Yes. Leveraging our manufacturing bases in China and Thailand, we supply projects globally. We also provide remote video guidance, optional on-site engineering supervision, and a rapid 2-hour response after-sales service.
Yes, we design and build ISO Class 4 to 8 environments that strictly adhere to international FDA, GMP, and CE regulations, ensuring your facility passes necessary validations.

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