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Modular Custom Cleanrooms

Modular Custom Cleanrooms

Modular Custom Cleanrooms

Fully assembled modular wall enclosure systems support full customization across the complete ISO 1–9 cleanliness spectrum, maintaining stable ISO Class 5 (Class 100) and ISO Class 6 (Class 1000) performance under both static and dynamic operating conditions. Two dedicated compliance design frameworks are provided to match different industrial verticals:
1.Biopharmaceutical & medical device configuration: Fully compliant with FDA 21 CFR Part 210 and 211 cGMP; complete DQ/IQ/OQ/PQ validation documentation packages are supplied to facilitate regulatory FDA audits.
2.Semiconductor & new energy configuration: Designed per ISO 14644 and SEMI industrial standards for comprehensive particulate and AMC abatement. Suitable for mass production lines in biopharmaceuticals, medical device manufacturing, semiconductor chip fabrication and new energy material processing.

Core Advantages

Core Advantages

Fast on-site assembly Standardized prefabricated wall, ceiling and air circulation modules cut overall project delivery lead times. Multi-stage gradient filtration enables rapid recovery of target cleanliness levels to sustain uninterrupted continuous mass production.
Full-range customizable environmental parameters Cleanliness classification, setpoint temperature, relative humidity and room differential pressure are all fully adjustable. Positive-pressure barrier design blocks ingress of external airborne contaminants, simultaneously satisfying low-particulate requirements for electronics manufacturing and microbial control thresholds for biopharmaceutical production.
Multi-industry applicable structural design HEPA and ULPA filter combinations are sized and configured to match target cleanliness ratings. Surface finishing options are differentiated by industry: static-dissipative coatings for semiconductor production workshops and seamless sterile coatings for biopharmaceutical facilities.
Expandable modular combination mode Each newly added functional zone is equipped with an independent dedicated air handling unit to avoid degradation of overall cleanliness performance during facility expansion. The scalable architecture supports capacity expansion for pharmaceutical manufacturers and iterative process upgrades for semiconductor fabs.