Process Control for Influenza A+B Assay. 2mL

• Developed for Lyra Real-Time PCR Assays
• Provides Dedicated External Process Validation Baselines
• Ensures Target Matrix Reagent Performance Tracking
• Storage Refrigerated at 2°C to 8°C
• Longevity Up to 24 Months Shelf Life .

The Quidel Lyra Process Control is a ready-to-use validation fluid used with Lyra Influenza A+B Assay. This 2ml external quality control material is formulated to assist high-complexity molecular laboratories in monitoring the execution of diagnostic runs. By processing this control parallel to active patient specimens, clinical teams can track procedural variables, safeguard baseline accuracy, and confirm systematic reagent integrity across multiple multiplex assay suites.

✦ ✦ ✦ FEATURES ✦ ✦ ✦

• Assay Integration: Validated exclusively as an external tracking component paired with Lyra Influenza A+B assay.
• Testing Mechanism: Functions as a comprehensive baseline control that must undergo the same clinical preparation and nucleic acid extraction steps as raw patient samples.
• Thermal Management: Engineered to remain functional and chemically stable without freezing when housed inside standard laboratory refrigeration between 2°C and 8°C.
• Extended Lifespan: Built to maintain precise product characteristics for up to a 24-month duration from its original date of production.

Utilize the Quidel Process Control for Influenza A+B Assay to align your laboratory with direct manufacturer standards, verify molecular extraction throughput, and maintain high diagnostic accuracy.

WARNING: This product can expose you to chemicals known to the State of California to cause cancer. For more information, go to www.P65Warnings.ca.gov.