Tag Archives: Audit MicroControls

October 2022—Audit MicroControls has announced the availability of its Linearity LQ hs-CRP for Ortho Vitros. The product is intended to simulate human patient serum samples for determining linearity, calibration verification, and verification of the reportable range for hs-CRP. The product consists of five levels of human serum and has an open-vial stability of five days when stored at 2° to 8°C.

April 2019—Audit MicroControls announced several additions to its line of calibration verification/linearity and daily quality control products. The company’s galectin-3 linearity and control kits are for use with quantitative assays on clinical laboratory analyzers, simulating human patient samples.

July 2014—Audit MicroControls added ready-to-use vitamin D linearity and control kits to its line of calibration verification/linearity and daily quality control products. These liquid, human serum–based products are intended for use with quantitative assays on clinical laboratory analyzers, simulating human patient serum samples. The Linearity LQ Vitamin D (universal) and Linearity LQ Vitamin D Roche both have five levels that demonstrate a linear relationship to each other when assayed for vitamin D, have a shelf life of two years, and an open-vial stability of 14 days when stored at 2°–8°C.

April 2014—Audit MicroControls added to its line of products the Control LQ Glycohemoglobin A1c—a liquid bi-level reference control consisting of human blood–based solutions.

April 2014—Audit MicroControls launched a new Web site, adding online ordering, access to Auditor QC, peer review data retrieval, and search functions by instrument, analyte, or indication. It also offers information about quality control products, calibration verification/linearity products, Audit Ship, and Audit Faxback.

March 2014—Audit MicroControls added the Linearity FD D-Dimer PathFast Immunoanalyzer, five levels, to its line of calibration verification/linearity products. It is intended to simulate human patient serum samples for the purpose of determining linearity, calibration verification, and verification of reportable range for D-dimer.

Audit MicroControls has added Control LQ Spinal Fluid to its line of daily quality control products. This bi-level reference control consisting of human serum-based solutions simulates patient spinal fluid samples for monitoring the precision of laboratory testing procedures for chloride, glucose, IgA, IgG, IgM, lactate, LDH, microalbumin, microprotein, and sodium.

Audit MicroControls’ Linearity FD General Chemistry Beckman AU simulates human patient serum samples for determining linearity, calibration verification, and verification of reportable range for albumin, alkaline phosphatase, ALT, total amylase, AST, total bilirubin, direct bilirubin, BUN, calcium, chloride, cholesterol, CO2, creatine kinase, creatinine, gamma-GT, glucose, iron, lactate, LDH, lipase, magnesium, phosphorous, potassium, sodium, total protein, triglycerides, and uric acid. This five-level lyophilized product, packaged as 10 × 5 mL, has a shelf life of two years and open-vial stability of seven days when stored at 2°C to 8°C.

Audit MicroControls received 510(k) clearance from the FDA, allowing the addition of assayed lithium to Audit’s therapeutic drug monitoring daily quality control and calibration verification/linearity kits. With the addition of lithium, Audit’s TDM linearity kit will have five levels and 14 assayed analytes and the control will have three levels and 13 assayed analytes.

Audit MicroControls has updated its logo, mission statement, and social media campaign. Audit’s mission is to supply daily QC and calibration verification/linearity materials to clinical labs worldwide while providing support, real-time data-reduction tools, same-day shipping, and quality products at a fair price.

Audit MicroControls has added to its line of calibration verification/linearity products, the beta-hydroxybutyric acid linearity, five levels. The control is intended to simulate human patient serum samples for determining linearity, calibration verification, and verification of reportable range for beta-hydroxybutyric acid. Packaged as 5 × 1 mL, this liquid product has a shelf life of two years and an open-vial stability ...

Audit MicroControls’ MicroLQ serum protein control, two levels, is intended to simulate human patient serum samples to monitor the precision of laboratory testing procedures for albumin, alpha1-acid glycoprotein, alpha1-antitrypsin, alpha2-macroglobulin, antithrombin, beta2 microglobulin, ceruloplasmin, complement C3, complement C4, haptoglobin, immunoglobulin A, immunoglobulin E, immunoglobulin G, immunoglobulin M, prealbumin, total protein, and transferrin.

Audit MicroControls’ MicroFD urine chemistry control, two levels, is intended to simulate human patient samples for monitoring the precision of laboratory testing procedures for urine chemistry assays, including amylase, calcium, chloride, creatinine, glucose, magnesium, microalbumin, microprotein, phosphorous, potassium, sodium, urea nitrogen, and uric acid.