Lipid & Cardiovascular Risk Assessment
Clinical chemistry solutions for cholesterol and lipid profile testing.
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Quality Control Materials
AV-QCLIP AV-QC Lipids Specialized (Multi-Level Liquid Control)
Specialized multi-level liquid quality control for lipid assays (Total Cholesterol, Triglycerides, HDL-Cholesterol, LDL-Cholesterol and related parameters). Human-matrix based with extended open-vial stability. Designed by Aurevant Medical for precise monitoring of lipid methods used in cardiovascular risk assessment.
No approved datasheet is available for this product yet.
Product Overview
Overview
The Aurevant AV-QC Lipids Specialized is a liquid, ready-to-use multi-level quality control material formulated specifically for the monitoring of precision and accuracy of lipid assays. It is intended for use with enzymatic methods that measure Total Cholesterol, Triglycerides, Direct HDL-Cholesterol, Direct LDL-Cholesterol and related calculated or measured lipid parameters.
The control is prepared in a human serum matrix to provide good commutability with patient samples. Being liquid and ready-to-use, it eliminates reconstitution steps and reduces the risk of preparation errors. After opening, the material offers extended open-vial stability when stored at 2–8 °C, supporting consistent daily or batch-wise quality-control practices.
Assayed target values and acceptable ranges are provided on a lot-specific value sheet for each level. The control is optimized for use with the Aurevant AV-Lipid Panel Kit and other Aurevant chemistry reagents on AV-Chem series analyzers, and is also suitable for other open-system lipid methods 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 control is prepared in a human serum matrix to provide good commutability with patient samples. Being liquid and ready-to-use, it eliminates reconstitution steps and reduces the risk of preparation errors. After opening, the material offers extended open-vial stability when stored at 2–8 °C, supporting consistent daily or batch-wise quality-control practices.
Assayed target values and acceptable ranges are provided on a lot-specific value sheet for each level. The control is optimized for use with the Aurevant AV-Lipid Panel Kit and other Aurevant chemistry reagents on AV-Chem series analyzers, and is also suitable for other open-system lipid methods 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
- •Specialized multi-level control dedicated to lipid assays
- •Human serum matrix for improved commutability with patient samples
- •Ready-to-use liquid format – no reconstitution required
- •Assayed for Total Cholesterol, Triglycerides, HDL-Cholesterol and LDL-Cholesterol
- •Extended open-vial stability at 2–8 °C
- •Lot-specific target values and acceptable ranges supplied
- •Ideal companion control for the Aurevant AV-Lipid Panel Kit
- •Supports daily precision monitoring and Levey-Jennings charting
- •Compatible with Aurevant AV-Chem analyzers and other open-system lipid methods after validation
- •Covers normal, borderline and elevated lipid concentration ranges
Key advantages
- •Specialized formulation focused on lipid assays improves relevance and performance monitoring compared with general chemistry controls
- •Liquid format eliminates reconstitution variability and preparation time
- •Human serum matrix enhances commutability with real patient specimens
- •Extended open-vial stability supports efficient daily QC without frequent bottle changes
- •Assayed values enable immediate use for monitoring and troubleshooting of lipid methods
- •Designed as the ideal companion control for the Aurevant AV-Lipid Panel Kit and related reagents
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, turbidity or precipitation is observed. 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 equilibrate to 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 Lipids Specialized – liquid ready-to-use multi-level quality control for Total Cholesterol, Triglycerides, HDL and LDL. Human-matrix, extended open-vial stability. Ideal companion for the Aurevant AV-Lipid Panel Kit.
Use Cases
Applications
- →Daily quality control of lipid profile assays
- →Monitoring of Total Cholesterol, Triglycerides, HDL-Cholesterol and LDL-Cholesterol methods
- →Precision and accuracy verification for cardiovascular risk assessment testing
- →Levey-Jennings charting and application of laboratory QC rules
- →Use on fully automated and semi-automated clinical chemistry analyzers
Approved documentation
Downloads
No approved documents are currently associated with this product.
Product questions
Frequently Asked Questions
Which lipid analytes does this control cover?
The control is assayed for Total Cholesterol, Triglycerides, HDL-Cholesterol, LDL-Cholesterol and related lipid parameters as listed on the lot-specific value sheet.
Is it ready to use?
Yes. It is a liquid, ready-to-use control. No reconstitution is required.
How many levels are available?
The product is supplied as a multi-level control (typically two or three levels covering normal, borderline and elevated ranges). Exact configuration is stated on the product label.
What is the open-vial stability?
After opening, the control typically remains stable for 14–30 days when stored at 2–8 °C. The exact claim is provided on the package insert and value sheet for each lot.
Is it suitable for use with the Aurevant AV-Lipid Panel Kit?
Yes. It is specifically designed as the companion quality control for the Aurevant AV-Lipid Panel Kit and related lipid reagents.
Can it be used on non-Aurevant analyzers?
Yes, after the laboratory has verified the suitability of the assigned values and matrix for the specific lipid methods in use.
How should the control be mixed before use?
Gently invert the bottle several times to ensure homogeneity. Avoid vigorous shaking that may introduce bubbles.
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