A clean room HVAC (Heating, Ventilation, and Air Conditioning) system in a pharmaceutical factory is specifically designed to maintain an ultra-clean environment with precise temperature, humidity, and air purity control. This is critical for manufacturing processes where the slightest contamination can compromise product quality and safety.| Product Name | Clean room HVAC system |
| Service Items | Project Design,Equipment production,installation and debugging |
| Color | White,blue or customized |
| Heat transfer mode | Fan cooler,water well cooler,water tower |
| Air clean grade | Class 100-1000000 |
| Standard | CE,ISO9001 |
| Humidity control | 5%~90% |
| Application | Pharmacy,factory,hospital,Laboratory, etc. |
In a pharmaceutical clean room, the HVAC system typically includes:
Air Filtration: The system uses multiple stages of HEPA (High-Efficiency Particulate Air) filters and sometimes ULPA (Ultra-Low Penetration Air) filters that can remove particles as small as 0.3 microns or even smaller, ensuring that the air inside the clean room remains virtually particle-free.
Air Pressurization Control: Clean rooms are maintained at positive pressure relative to surrounding areas to prevent unfiltered air from entering. Pressure differentials are closely monitored and controlled.
Temperature and Humidity Control: Precise control of temperature and humidity levels are essential as they can affect both the manufacturing process and the stability of pharmaceutical products.
Air Changes per Hour (ACH): A high number of air changes per hour (usually ranging from 50 to over 200) ensures that airborne contaminants are rapidly flushed out of the room.
Air Distribution: Laminar or turbulent airflow patterns are designed to minimize turbulence and reduce the risk of particle migration.
Air Recirculation: The HVAC system continuously circulates and re-filters the air within the clean room to maintain the required cleanliness level.
Bypass Systems: Some HVAC systems may include a bypass mode for when the clean room is not in use, which saves energy without compromising the sterility of the space.
Validation and Monitoring: The entire HVAC system must be validated and continuously monitored to ensure it's functioning within predefined parameters.
Separate Supply and Exhaust Ducts: To prevent cross-contamination, supply and exhaust ducts are separate and strategically placed.
