What is the HVAC System in a Cleanroom?
A cleanroom HVAC system is a special air-handling system. It is made to control contamination. This system regulates air cleanliness, airflow, pressure, temperature, and humidity in a specific area.
Unlike comfort HVAC, cleanroom HVAC is process-critical—it directly affects product quality, compliance, and safety.
Core Objectives of Cleanroom HVAC
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Control airborne particles (dust, microbes)
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Maintain pressure differentials between rooms
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Provide uniform, controlled airflow
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Hold tight temperature & humidity limits
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Prevent cross-contamination
Key Components of a Cleanroom HVAC System
1️⃣ Air Handling Unit (AHU)
Cleanroom AHUs are engineered for:
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High air change rates
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Tight temperature & RH control
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Multistage filtration (pre-filter → fine filter)
What’s special:
Leak-tight casing, smooth internal surfaces, easy cleaning access.
2️⃣ HEPA / ULPA Filtration
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HEPA: ≥99.97% efficiency at 0.3 µm
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ULPA (where required): higher efficiency
Installed at:
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AHU outlet (terminal housings), or
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Ceiling terminals in critical zones
Purpose: Deliver ultra-clean air directly to the process area.
3️⃣ Airflow Pattern (How Air Moves)
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Laminar (Unidirectional) Flow
Used in critical zones (e.g., filling lines). Air moves uniformly downward, sweeping particles away. -
Turbulent (Non-unidirectional) Flow
Used in background areas with controlled mixing.
Correct airflow = correct cleanliness.
4️⃣ Pressure Cascade
Cleanrooms use pressure differentials to block contamination.
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Positive pressure: Cleaner area → dirtier area
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Negative pressure: For hazardous/potent processes
Typical differential: 5–15 Pa between adjacent rooms.
5️⃣ Temperature & Humidity Control
Common pharma ranges:
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Temperature: 20–25 °C
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Relative Humidity: process-specific (often 40–60%)
Why it matters:
Product stability, operator comfort, and electrostatic control.
6️⃣ Air Changes per Hour (ACH)
Cleanrooms use very high air change rates to dilute and remove contaminants.
Typical ranges (indicative):
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ISO 8 / Grade C: 20–30 ACH
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ISO 7 / Grade B: 40–60 ACH
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ISO 5 / Grade A: 200+ ACH (laminar zones)
Cleanroom HVAC vs Comfort HVAC (Quick Comparison)
| Aspect | Comfort HVAC | Cleanroom HVAC |
|---|---|---|
| Purpose | Human comfort | Contamination control |
| Filtration | Basic | HEPA / ULPA |
| Air Changes | Low | Very high |
| Pressure Control | Minimal | Critical |
| Validation | Not required | Mandatory |
Where Cleanroom HVAC Is Used
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Pharmaceutical manufacturing
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Biotechnology & laboratories
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Medical device production
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Semiconductor & electronics
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Food & nutraceutical facilities
Why Execution & Commissioning Matter
In cleanrooms:
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A small air leak can fail validation
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Poor balancing can break pressure cascade
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Incorrect HEPA installation can invalidate the room
That’s why cleanroom HVAC systems require:
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Precise installation
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Thorough testing
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Documented commissioning & validation support
In Simple Words
A cleanroom HVAC system is a contamination-control machine—not just an air conditioner.
It creates a clean, stable, and controlled environment where sensitive products can be safely manufactured.Get a Future-Ready HVAC System in a Cleanroom Today
Planning a large commercial or institutional project? Get in touch with Vipul HVAC House, Gujarat’s trusted HVAC Site Works (SITC) contractor.
📞 Call: +91 9825636606
📧 Email: vipulaircondition@gmail.com
🌐 Visit: www.vipulac.inVipul AC – Gujarat’s Expert in HVAC System in a Cleanroom.
