Clean Room HVAC Systems
ISO Certified Contamination Control
System Overview
Clean Room HVAC systems are specialized environmental control solutions for pharmaceutical, biotechnology, semiconductor, and medical device manufacturing. These systems maintain extremely low levels of airborne particles, precise temperature (±0.5°C), and strict humidity control (40-60% RH). They incorporate HEPA/ULPA filters, laminar or turbulent airflow patterns, pressure cascades, and air change rates from 20 to over 600 per hour. Cleanroom HVAC is designed to meet ISO 14644 standards and regulatory requirements like GMP, FDA, and EU guidelines, ensuring product quality and patient safety.
Key Features
HEPA/ULPA filtration (H13/H14/U15)
Precise temperature control (±0.5°C)
Precise humidity control (±5% RH)
Positive or negative pressure cascade
Air change rates: 20-600+ ACH
Laminar or turbulent airflow
GMP, ISO 14644, FDA compliant
Redundant AHUs for 24/7 operation
Stainless steel or epoxy-coated construction
Real-time particle and environmental monitoring
Key Benefits
- Contamination-free manufacturing environment
- Meets international regulatory standards
- Product quality and safety assurance
- Worker and product protection
- Energy-optimized design for cleanrooms
- Validated performance documentation
- Reduced risk of batch rejection
- Comprehensive alarm and data logging
Technical Specifications
ISO Class: 5, 6, 7, 8
Particle Count: As per ISO 14644
Air Changes: 20 to 600+ ACH
HEPA Efficiency: 99.97% to 99.9995%
Temperature: 20-24°C ±0.5°C
Humidity: 40-60% ±5%
Pressure: Positive or Negative
Ideal Applications
Pharmaceutical Manufacturing
Biotechnology Labs
Semiconductor Fabrication
Medical Device Assembly
Hospital Pharmacies (IV admixture)
Food Processing (aseptic areas)
Cosmetics Manufacturing