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 temperature monitoring 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 types of data logging devices are utilized in the Biotech industry for long-term temperature and humidity monitoring purposes. These devices facilitate documented environmental conditions throughout the storage of critical materials. Unnoticed temperature and 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 calibration of all data logging devices using high accuracy, NIST traceable PRT (Platinum Resistance Thermometer) and humidity calibration standards. Our PRTs uphold industry leading accuracies of up to 0.025 degrees Celsius. Our humidity probes also 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 data logging devices 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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