Routine Clinical Chemistry
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Quality Control Materials
AV-QCNP AV-QC Chemistry Normal & Pathological (2-Level Liquid Control)
Liquid, ready-to-use two-level (Normal and Pathological) multi-analyte quality control for routine clinical chemistry. Human-matrix based, extended open-vial stability, assayed for more than 25 common chemistry analytes. Designed by Aurevant Medical for reliable daily QC on automated and semi-automated analyzers.
No approved datasheet is available for this product yet.
Product Overview
Overview
The Aurevant AV-QC Chemistry Normal & Pathological is a liquid, ready-to-use two-level quality control material intended for the monitoring of precision and accuracy of routine clinical chemistry assays. The set provides a Normal (Level 1) and a Pathological (Level 2) control that together span the clinically relevant concentration ranges for more than 25 frequently measured analytes, including metabolites, enzymes, lipids, proteins and selected electrolytes.
The controls are prepared from a human serum matrix to improve commutability with patient samples. Being liquid and ready-to-use, they eliminate reconstitution steps and reduce the risk of preparation errors. After opening, the controls demonstrate extended open-vial stability when stored at 2–8 °C, supporting efficient daily QC practices.
Assayed target values and acceptable ranges are provided for each analyte on a lot-specific value sheet. The controls are designed for use with Aurevant chemistry reagents on AV-Chem series analyzers and are also suitable for other open-system clinical chemistry instruments after laboratory validation.
This product is an original Aurevant Medical quality control material manufactured under controlled conditions and intended for professional laboratory use by trained personnel.
The controls are prepared from a human serum matrix to improve commutability with patient samples. Being liquid and ready-to-use, they eliminate reconstitution steps and reduce the risk of preparation errors. After opening, the controls demonstrate extended open-vial stability when stored at 2–8 °C, supporting efficient daily QC practices.
Assayed target values and acceptable ranges are provided for each analyte on a lot-specific value sheet. The controls are designed for use with Aurevant chemistry reagents on AV-Chem series analyzers and are also suitable for other open-system clinical chemistry instruments after laboratory validation.
This product is an original Aurevant Medical quality control material manufactured under controlled conditions and intended for professional laboratory use by trained personnel.
Product name and code identify the record only; they are not a substitute for current manufacturer documentation. Confirm intended use, configuration, availability, supported applications, and all technical and commercial terms in writing before procurement.
Key Features
Features
- •Two-level (Normal and Pathological) liquid control in a single convenient set
- •Human serum matrix for improved commutability with patient samples
- •Ready-to-use liquid format – no reconstitution required
- •Assayed for more than 25 common clinical chemistry analytes
- •Extended open-vial stability at 2–8 °C
- •Lot-specific target values and acceptable ranges supplied
- •Suitable for daily precision monitoring and Levey-Jennings charting
- •Optimized for use with Aurevant chemistry reagents and AV-Chem analyzers
- •Compatible with other open-system clinical chemistry instruments after validation
- •Supports both routine and pathological concentration ranges in one product
Key advantages
- •Single two-level product covers both normal and pathological ranges, simplifying inventory
- •Liquid format eliminates reconstitution variability and preparation steps
- •Human serum matrix improves commutability compared with some artificial controls
- •Extended open-vial stability supports efficient daily QC without frequent bottle changes
- •Assayed values enable immediate use for precision monitoring and troubleshooting
- •Fully compatible with Aurevant reagent systems and open-platform analyzers
Sample Types
- →Not applicable (quality control material)
Safety
Safety Information
For in-vitro diagnostic use only. This product contains human-source material. Although donor units were tested and found non-reactive for common infectious disease markers, handle as potentially infectious. Wear appropriate personal protective equipment (gloves, lab coat, eye protection). Store at 2–8 °C; do not freeze. Do not use after the expiry date. After opening, observe the stated open-vial stability period and discard if contamination is suspected. Dispose of according to local laboratory and environmental regulations. Consult the package insert and Safety Data Sheet (SDS) before use.
Instructions
Directions for Use
Remove the control bottles from refrigerated storage (2–8 °C) and allow them to reach room temperature or the temperature required by the analyzer if specified.
Technical Data
Specifications
Specifications
Research Status
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Publication Approval
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Technical Specification Status
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Specification
Aurevant AV-QC Chemistry Normal & Pathological – liquid ready-to-use two-level (Normal/Pathological) multi-analyte quality control for routine clinical chemistry. Human-matrix, extended open-vial stability, assayed for 25+ analytes.
Use Cases
Applications
- →Daily quality control of routine clinical chemistry assays
- →Monitoring of analytical precision and accuracy
- →Levey-Jennings charting and Westgard rule application
- →Verification of calibration and reagent performance
- →Use on fully automated and semi-automated clinical chemistry analyzers
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View applicationApproved documentation
Downloads
No approved documents are currently associated with this product.
Product questions
Frequently Asked Questions
How many levels are included?
Two levels: Normal (Level 1) and Pathological (Level 2).
Is the control liquid or lyophilized?
It is a liquid, ready-to-use control. No reconstitution is required.
How many analytes are assayed?
More than 25 routine clinical chemistry analytes are typically assigned. The exact list and values are provided on the lot-specific value sheet.
What is the open-vial stability?
After opening, the controls typically remain stable for 14–30 days when stored at 2–8 °C. The exact claim is stated on the package insert and value sheet for each lot.
Is the matrix human-based?
Yes. The controls are prepared from a human serum matrix to improve commutability with patient samples.
Can these controls be used with non-Aurevant reagents?
They are optimized for Aurevant reagents on AV-Chem analyzers. Use with other reagent systems requires laboratory verification of the assigned values and suitability.
How should the controls be handled before use?
Allow the bottles to equilibrate to the appropriate temperature, mix gently by inversion, and load them onto the analyzer in the same manner as patient samples.
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