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- AMPLIRUN® Total SARS-CoV-2/FluA/FluB/RSV Control (Swab), 10 x 500 µL
The Vircell AMPLIRUN® Total SARS-CoV-2/FluA/FluB/RSV Control is an external quality control panel designed for nucleic acid detection of four major respiratory pathogens: SARS-CoV-2, Influenza A (H3N2), Influenza B, and Respiratory Syncytial Virus (RSV). Formulated in a swab transport medium to mimic clinical respiratory specimens, this control ensures non-infectious, safe, and reliable use across molecular diagnostic platforms.
By incorporating complete viral genomes, this control validates both nucleic acid extraction and amplification, enabling reproducibility, long-term quality monitoring, and compliance with accreditation standards.
Available Control
| Product Reference | Description | Volume | Nº Vials | Class |
|---|---|---|---|---|
| MBTC031 | AMPLIRUN® Total SARS-CoV-2/FluA/FluB/RSV Control (Swab) | 500 µL | 10 single-use vials | CE |
Panel Composition
- SARS-CoV-2
- Influenza A (H3N2)
- Influenza B
- Respiratory Syncytial Virus (RSV)
Key Features
- Complete inactivated microorganisms – includes four clinically relevant respiratory pathogens.
- External quality control – verifies both extraction and amplification stages.
- Respiratory swab matrix – simulates real clinical samples for realistic assay validation.
- Quantified control – ensures consistent and reproducible results.
- Non-infectious & lyophilized – safe, stable, and reduces shipping/transportation costs.
- Single-use vials – 10 lyophilized vials for convenient use and contamination control.
- Sequencing data available – facilitates probe and primer design.
Applications
- External quality control for multiplex molecular assays detecting SARS-CoV-2, Influenza A, Influenza B, and RSV.
- Validation and verification of PCR/qPCR diagnostic assays and panels.
- Long-term performance monitoring of extraction and amplification workflows.
- Quality assurance for reagents, assay batches, and instrument consistency.
- Training and competency assessment of laboratory personnel.
- Troubleshooting assay failures and suspect results.
- Meeting compliance requirements for laboratory accreditation.
Product Details
| Property | Value |
|---|---|
| Volume per vial | 500 µL |
| Nº Vials | 10 single-use lyophilized vials |
| Format | Inactivated whole microorganisms in transport medium |
| Infectivity | Non-infectious |
| Class | CE |
| Pathogens | SARS-CoV-2, Influenza A H3N2, Influenza B, Respiratory Syncytial Virus |
| Storage | Stable at ambient temperature until reconstituted |
The AMPLIRUN® Total SARS-CoV-2/FluA/FluB/RSV Control provides laboratories with a standardized and reliable external quality control for molecular detection of four key respiratory pathogens. With inactivated microorganisms in a swab matrix, quantified genomes, and lyophilized stability, this panel is indispensable for assay validation, quality assurance, and regulatory compliance in molecular diagnostics and clinical virology.
The Vircell AMPLIRUN® Total SARS-CoV-2/FluA/FluB/RSV Control is an external quality control panel designed for nucleic acid detection of four major respiratory pathogens: SARS-CoV-2, Influenza A (H3N2), Influenza B, and Respiratory Syncytial Virus (RSV). Formulated in a swab transport medium to mimic clinical respiratory specimens, this control ensures non-infectious, safe, and reliable use across molecular diagnostic platforms.
By incorporating complete viral genomes, this control validates both nucleic acid extraction and amplification, enabling reproducibility, long-term quality monitoring, and compliance with accreditation standards.
Available Control
| Product Reference | Description | Volume | Nº Vials | Class |
|---|---|---|---|---|
| MBTC031 | AMPLIRUN® Total SARS-CoV-2/FluA/FluB/RSV Control (Swab) | 500 µL | 10 single-use vials | CE |
Panel Composition
- SARS-CoV-2
- Influenza A (H3N2)
- Influenza B
- Respiratory Syncytial Virus (RSV)
Key Features
- Complete inactivated microorganisms – includes four clinically relevant respiratory pathogens.
- External quality control – verifies both extraction and amplification stages.
- Respiratory swab matrix – simulates real clinical samples for realistic assay validation.
- Quantified control – ensures consistent and reproducible results.
- Non-infectious & lyophilized – safe, stable, and reduces shipping/transportation costs.
- Single-use vials – 10 lyophilized vials for convenient use and contamination control.
- Sequencing data available – facilitates probe and primer design.
Applications
- External quality control for multiplex molecular assays detecting SARS-CoV-2, Influenza A, Influenza B, and RSV.
- Validation and verification of PCR/qPCR diagnostic assays and panels.
- Long-term performance monitoring of extraction and amplification workflows.
- Quality assurance for reagents, assay batches, and instrument consistency.
- Training and competency assessment of laboratory personnel.
- Troubleshooting assay failures and suspect results.
- Meeting compliance requirements for laboratory accreditation.
Product Details
| Property | Value |
|---|---|
| Volume per vial | 500 µL |
| Nº Vials | 10 single-use lyophilized vials |
| Format | Inactivated whole microorganisms in transport medium |
| Infectivity | Non-infectious |
| Class | CE |
| Pathogens | SARS-CoV-2, Influenza A H3N2, Influenza B, Respiratory Syncytial Virus |
| Storage | Stable at ambient temperature until reconstituted |
The AMPLIRUN® Total SARS-CoV-2/FluA/FluB/RSV Control provides laboratories with a standardized and reliable external quality control for molecular detection of four key respiratory pathogens. With inactivated microorganisms in a swab matrix, quantified genomes, and lyophilized stability, this panel is indispensable for assay validation, quality assurance, and regulatory compliance in molecular diagnostics and clinical virology.
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