Knowing the proper compressed air quality level required when considering FDA enforced cGMP is important. There are a variety of standards that govern compressed air and the quality of air required throughout a compressed air system can vary. TRI can assist you with with testing the compressed air quality for every application from direct product contact to indirect product contact and USP 797 contains requirements for the operations of clean rooms. We can also assist you with setting up a custom compressed air quality program for your company. TRI recommends developing a compressed air quality program for validation that is repeatable for verification and compliance for FDA enforced cGMP.

We offer quality, reliable 24 hour results*, detailed laboratory reports and excellent customer service. TRI's quality system is in compliance with ISO/IEC 17025 General Requirements for the Competence of Testing and Calibration Laboratories and with ANSI/ISO/ASQ 9001-2000 Quality Management Systems Requirements.

Once your samples are returned for 24 hour analysis*, your results will be available through our online report access but if you need your results emailed just ask! If you need faster than 24 hour turnaround just let us know. TRI's accredited laboratory can perform a compressed air analysis of your compressor, validation or process air.

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* If your specification requires a breakdown of oil mist from particulate a 48 hour turnaround is required to meet this specification.