IETQAN conducts meticulous cleanroom HVAC validations in accordance with ISO 14644 requirements, ensuring critical processes are executed under controlled conditions in the medical device and pharmaceutical industries. Our team of experts carries out a range of tests, including particulate count/classification, air flow measurement, air pressure difference test, temperature test, and humidity test to ensure your cleanroom meets industry standards and regulatory requirements.
Choose IETQAN for your clean room validation needs and experience peace of mind knowing your critical processes are executed under controlled conditions.