Clean Room Validation / HVAC Validation
Heating ventilation and air conditioning is an integral component in pharmaceutical, Biotechnology, Hospitals, Aerospace, Automotive and semiconductor facility functionality.
Validation of HVAC is an essential subject to provide documented evidence about the accuracy of results produce by it.The various parameter to be evaluated for HVAC validations are Airflow velocity, Air changes per hour, Filter leak test, Non viable particle count,Recovery test, Temperature humidity test, Pressure difference test, Air flow pattern with videography.
We Carries out following tests to validate clean rooms/clean zones.
We conduct Air Velocity Measurement / tests to determine the average filter face velocity and uniformity, and the average room airflow velocity and uniformity within a clean room.
We conduct complete filter integrity testing services. These are offered for both the Pharmaceutical and Microelectronics industries. We are equipped to perform HEPA Filter Integrity Test Poly Alpha Olefin (PAO) depending on client-facility's specific requirements.
Our Particle Count Test provides complete airborne particle count cleanliness classification. The test is performed to determine the actual particle count level within the facility at the time of the test.
We conduct validation tests that include Temperature and Humidity Measurements / Tests. The general level test is used to ensure that the clean rooms HVAC system maintaince the specifed levels of temperature / humidity required for both occupant comfort and process temperature control.
We conduct Room Pressure balancing test for industrial clean rooms. As a part of the validation process, this test verifies that a pressure differential meet the specified requirements.
It is performed to determine whether the clean room or clean zone is capable of returning to it specified cleanliness class within a defined time after being exposed to a source of airborne particulate challenge inform of smoke or aerosol.
