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.

Laboratory cold rooms facilitate the storage of many critical materials that demand constant temperature and security. Unnoticed cold room temperature excursions can have a serious effect on the quality of your product and may result in loss of expensive product.

Biometrix provides on-site cold room calibration using high accuracy, NIST traceable PRT (Platinum Resistance Thermometer) calibration standards. Our PRTs uphold industry leading accuracies of up to 0.025 degrees Celsius. 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 cold rooms with temperature monitoring configurations ranging from stand-alone temperature gauges to advanced central monitoring systems 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 cold room validation


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