Clean Room
Validation
Clean room validation is a process used to verify that controlled environments such as pharmaceutical, operation theaters, data center, drug preparation area and electronics industries to meet stringent cleanliness and contamination control standards. This involves testing the room’s ability to maintain specific conditions including HEPA filter testing, Air Velocity, particle counts, Microbial contaminants temperature, humidity and airflow patterns.
Validation procedure is carried out by using specified equipment to monitor and measure these parameters to ensure they adhere to regulatory requirements. Successful clean room validation prevents contamination, ensuring product quality and maintaining safety standards. It ensures that the environment supports the intended processes and maintains the integrity of sensitive operations.
- Clean room classification by particle count HEPA
- Filter Integrity Test
- Particle Count Test
- Air Velocity Test
- Air Change Rate Calculation
- Sound Level Test
- Light Intensity Test
- Temperature & Relative Humidity Test
- Air Sample -Total Bacterial Count and Total fungal Count
Duct Cleanliness
Verification Test
by NADCA
Clean duct verification is a process used to ensure that air ducts in HVAC systems are free from contaminants and functioning efficiently. This involves inspecting and testing ducts for cleanliness and integrity, often using specialized tools such as video inspection using cameras and airflow measurement devices. The verification process assesses the presence of dust or debris that could affect air quality and
system performance. By confirming that ducts are clean and properly maintained, clean duct verification helps prevent the spread of pollutants, improves indoor air quality and enhances the overall efficiency of the HVAC system. It is essential for maintaining a healthy and comfortable indoor environment.