AMP 2019 Presentation

NeuMoDx™ Molecular recently presented the evaluation of DiaSorin Molecular Enterovirus (EV) Primer Pair and Cytomegalovirus (CMV) Primer Pair in Laboratory Developed Test (LDT) Implementation on the open, random-access NeuMoDx™ 288 Molecular System at the Association for Molecular Pathology’s conference held in Baltimore Maryland. Michelle Mastronardi (Director, Systems Integration at NeuMoDx Molecular), along with Stephen Young, Ph.D. (Director of Research and Clinical Trials TriCore Reference Laboratories), keynoted our workshop, speaking to the work they have performed utilizing our system firsthand and presenting their experiences. To view our latest presentation, please fill out the form below.

Coronavirus Assay Information

NeuMoDx™ Molecular, a sample-to-result molecular diagnostic company focused on providing testing solutions to hospital and commercial reference laboratories, has developed a SARS-CoV-2 Assay for use on the high throughput, fully automated NeuMoDx™ 288 and 96 Molecular Systems. The U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for the NeuMoDx™ SARS-CoV-2 Assay implemented on the NeuMoDx™ Molecular Systems.

To learn more about SARS-CoV-2 testing, click here.
To order, click here.