Periodic calibration verification is the only way to verify the accuracy of the entire reportable range for patient testing. Another important aspect of the laboratory is proficiency testing to meet laboratory regulations. When calibration verification procedures are coupled with peer review, laboratories can better prepare their labs for on-going proficiency testing. Verification of the new systems or reagents requires an assessment of linearity, accuracy and precision of the systems.

Ammonia/Ethanol CAL?VERŪ solutions are intended for in vitro diagnostic use in the quantitative determination of linearity, calibration verification, verification of theAnalytical Measurement Range (AMR), and verification of reportable ranges of manua

Enzyme Linearity Test Set solutions are intended for in vitro diagnostic use in the quantitative determination of enzyme linearity and Analytical Measurement Range (AMR) using automated, semi-automated and manual methods. The enzymes included in this

HDL Cholesterol CAL?VERŪ solution are intended for in vitro diagnostic use in the quantitative determination of linearity, calibration verification, verification of Analytical Measurement Range (AMR), and verification of reportable ranges of manual, a



Multi-Analyte CAL?VERŪ solutions are intended for in vitro diagnostic use in the quantitative determination of linearity, calibration verification, verification of Analytical Measurement Range (AMR) and verification of reportable ranges of automated

Refl ectance II Test Set solutions are intended for in vitro diagnostic use in the quantitative determination of linearity, calibration verifi cation, verifi cation of Analytical Measurement Range (AMR), and verifi cation of reportable ranges on clin

Salicylate CAL?VERŪ solutions are intended for in vitro diagnostic use in the quantitative determination of linearity, calibration verification, verification of Analytical Measurement Range (AMR) and verification of the reportable range on immunochem



TDM I CAL?VERŪ assayed solutions are intended for in vitro diagnostic use in the quantitative determination of linearity, calibration verification, verification of Analytical Measurement Range (AMR) and verification of reportable ranges on immunochemi

Total Protein/Albumin/Cholesterol CAL?VERŪ materials are intended for in vitro diagnostic use in the quantitative determination of linearity, calibration verification, verification of Analytical Measurement Range (AMR) and verification of reportable

Total bilirubin and direct bilirubin levels are measured directly in the blood, whereas indirect bilirubin levels are derived from the total and direct bilirubin measurements... >> read more