Iquum Gets FDA OK for Flu A/B Test; Eyes More Assays for Its Automated MDx System | GenomeWeb

By Ben Butkus

Clinical diagnostic test maker Iquum this week received US Food and Drug Administration clearance for its Liat Influenza A/B assay and fully automated and integrated Liat Analyzer.

Iguum said the real-time PCR-based test — its first 510(k) win — is designed to enable clinical labs to detect and differentiate influenza A and B in about 20 minutes, or about as fast as currently used immunoassays, but with the increased sensitivity afforded by nucleic acid testing.

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Mar
02
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This online seminar will highlight recent advances in the use of next-generation sequencing to detect drug-resistant mutations in patients with HIV or HCV. 

Mar
09
Sponsored by
Bio-Rad

This webinar will discuss how next-generation sequencing and digital PCR can be used in a complementary manner for liquid biopsies in order to improve patient care.