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 controllers offer advanced control and alarm functionality to facilitate the storage of critical materials that demand constant humidity set points 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 controller calibration using high accuracy, NIST traceable documenting process calibrators. Our documenting process calibrators enable Biometrix technicians to simulate inputs over the entire operating range of the controller at industry leading accuracies of up to 0.025% of instrument reading. 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 controllers 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.

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