OHVAC Validation (Clean Room services)
At VALQPRO LLP, we specialize in clean room validation to ensure contamination control, environmental stability, and regulatory compliance in pharmaceutical, biotech, and healthcare industries. Our services help maintain adherence to ISO 14644, EU GMP, US FDA, and WHO guidelines for clean room environments.
Air Velocity & Airflow Volume Measurement
Determines airflow distribution in clean rooms.
Ensures proper air changes per hour (ACH) for contamination control.
Uses high-precision anemometers for accurate velocity readings.
Filter Integrity Testing (HEPA & ULPA Filters)
Checks the efficiency of HEPA & ULPA filters in removing airborne contaminants.
Conducted using aerosol photometers & PAO/DOP testing.
Ensures filters are free from leaks and functioning as per GMP standards.
Non-Viable Particle Count (Environmental Monitoring)
Measures airborne particle concentration in clean rooms.
Ensures compliance with ISO 14644-1 class limits.
Uses laser particle counters to detect submicron particles.
Air Flow Direction Study (Smoke Visualization Test)
Determines unidirectional airflow and contamination control effectiveness.
Conducted using smoke tests with high-efficiency fog generators.
Smoke study is recorded using 8K high resolution Full HDR cameras.
Multi angle action cameras with 8K resolution (Study is being recorded from all four sides).
Smoke study is performed using Glycerol based smoke fogger and also water-based steam fogger according to requirement of the client.
Our expertise includes smoke study with video recording in static condition and also Dynamic condition (Interventions) with multi angle shoot.
We also provide clubbed video in one screen for multi angle camera.
Ensures airflow patterns comply with ISO & GMP standards.
Our validation process is performed using state-of-the-art equipment to deliver precise and reliable results. This ensures that your clean room environment meets industry regulations, minimizing contamination risks.