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Respiratory I Plus EQA/PT Scheme (Q4)
The Respiratory I Plus EQA will focus on the molecular detection and determination of various influenza A & B, respiratory syncytial virus strains and SARS-Cov-2. The panel is designed to represent various clinical scenarios. Participating laboratories will be expected to test each panel using their appropriate molecular methods and report their individual test results to QCMD.
Total Number of Challenges: 1
Number of Panel Members: 10
Distribution / Testing Period: Q4
| Sample NA Target Source | Cultured and/or Clinical material |
| Matrix Panel Format | Transport Medium |
| Panel Member Target Range | Covering clinical range |
| Panel Member Sample Volume | 1.0 ml |
| Panel Sample Pre-treatment Requirement | Ready for analysis. Treat as clinical samples and analyse accordingly. |
| Panel Analysis Type | Qualitative |
| Panel Testing | Evaluated by various molecular methodologies |
| Storage / Shipment Conditions | <-20°C / Frozen on Dry-ice |
| Accreditation / Regulatory Status | Accredited to ISO 17043 |
$1,398.42
