Our facility is equipped with world class instruments to carry out clean room validation activities. The critical parameters measurement such as differential pressure, positive pressure, negative pressure, air velocity, air volume, ACPH measurement, Air particle measurement, and DOP test for HEPA filters etc… can be performed as per Current Good Manufacturing Practice (cGMP) requirements.
Our scope of activities covers clean areas such as pass-through boxes, laminar flow hoods, classified clean rooms, sterile areas including healthcare facilities, pharmaceutical, hospitals and HVAC systems. Our team of trained personals ensure the cGMP requirements are met while performing validation activities within the critical areas.