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Humidity Chamber Calibration
Due to heightened quality requirements from regulatory bodies such as the FDA, from customers and from internal quality assurance guidelines, equipment calibration is more important than ever. As an FDA-regulated company, you may be audited for your compliance with FDA regulatory requirements – either GLP (Good Laboratory Practices) or GMP (Good Manufacturing Practices). The FDA requires that the display accuracy of all instruments that have an effect on the quality of your product be verified (calibrated) over a specified interval of time.

Many of today's humidity chambers are equipped with advanced control systems and alarms to facilitate the storage of critical materials that demand constant humidity setpoints and security. Unnoticed humidity excursions can have a serious effect on the quality of your product whether it be cell culture or clinical assay.

Biometrix provides on-site humidity chamber calibration using high accuracy, NIST traceable humidity probes. Our humidity probes uphold industry leading accuracies of up to 0.2%RH. This level of accuracy ensures 4:1 accuracy ratio compliance, even for customers who maintain the most stringent process tolerances. Upon completion of calibration, Biometrix technicians will leave you with detailed calibration certificates, with information on as-found data, as-left data, test point deviations, instrument tolerance and instrument operating range.

Our technicians have experience with a vast array of humidity chambers and can provide you with the high quality service that you demand. Our ultimate goal is to leave you with the peace of mind that your equipment is performing its role properly and accurately.

Biometrix also offers humidity chamber validation


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