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.

Spectrophotometers have a vital role in the measurement of absorbance and transmittance throughout R&D processes. It is critical that the functionality of these instruments is verified regularly. Unnoticed deviations can have a serious effect on the quality of your product whether it be cell culture or clinical assay

Biometrix provides on-site spectrophotometer calibration using high accuracy, NIST traceable cuvette standards. 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 spectrophotometers 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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