Mô tả
CLEANROOM CONSTRUCTION IN THE PHILIPPINES
Turnkey Consultation, Design & Build Services Backed by Over 12 Nationwide Branches
Achieving a world-class cleanroom doesn’t have to be complicated. As one of the leading Cleanroom Constructors in the Philippines, we deliver end-to-end cleanroom consultation, design, engineering, and turnkey construction for industries that demand precision- semiconductor, pharmaceutical, biotechnology, medical devices, research, aerospace, food manufacturing, and more.
With 12+ active branches nationwide, including Cavite, Batangas, Laguna, Manila, Baguio, Subic, Clark, and Cebu, we provide rapid deployment, localized support, and reliable project execution anywhere in the Philippines.
Why Clients Trust Us
Complete engineering & construction for controlled environments.
Precision-engineered cleanrooms meeting global standards.
Fast Deployment
Supported by 12+ branches across the Philippines.
Our Turnkey Cleanroom Services
We manage the entire build process, including:
- Cleanroom Doors & Windows
- Ceiling & Wall Panel Systems
- Cleanroom HVAC & Filtration Systems
- Cleanroom Equipment
- Cleanroom Flooring Solutions
- Cleanroom Performance Testing and Validation
Your cleanroom is delivered fully operational and ready for qualification.
Philippines Branch Network – 12+ Strategic Locations
Cavite Batangas Laguna Manila Baguio Subic Clark Cebu
Selecting the Right Cleanroom Class for Your Needs
Choosing the correct cleanroom classification is essential for compliance, process integrity, and long-term performance.
1. Nature of Your Process: Determine whether operations involve sensitive components, biological handling, or contamination-prone steps.
2. Product Sensitivity: Evaluate how particles, microbes, or environmental changes may affect yield or quality.
3. Regulatory Requirements: Operations may fall under FDA, cGMP, PIC/S, WHO, or EU GMP Annex 1.
4. Workflow & Operational Volume: High occupancy or frequent transfers may require stricter classifications.
5. Long-Term Scalability: Ensure the cleanroom supports expansion or tighter classifications in the future.
| Industry / Application |
Typical ISO Class |
| Semiconductor & Microelectronics |
ISO 3–6 |
| Medical Device Manufacturing |
ISO 6–7 |
| Pharmaceutical Compounding |
ISO 5–7 |
| Biotechnology & Cell Culture |
ISO 5–7 |
| General Manufacturing |
ISO 7–8 |
| R&D Laboratories |
ISO 7–8 |
| ISO Class |
Max Particles/m³ (≥0.1 µm) |
Max Particles/m³ (≥0.5 µm) |
| ISO 1 |
10 |
0 |
| ISO 2 |
100 |
2 |
| ISO 3 |
1,000 |
35 |
| ISO 4 |
10,000 |
352 |
| ISO 5 |
100,000 |
3,520 |
| ISO 6 |
1,000,000 |
35,200 |
| ISO 7 |
— |
352,000 |
| ISO 8 |
— |
3,520,000 |
| ISO 9 |
— |
35,200,000 |
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Philippines
