We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies. Cookie Policy.

Features Partner Sites Information LinkXpress
Sign In
Advertise with Us
GLOBETECH PUBLISHING LLC

Download Mobile App





Portable COVID-19 Test Instrument Uses Bulk Acoustic Wave Technology to Achieve SARS-CoV-2 Antigen Testing in 20 Minutes

By LabMedica International staff writers
Posted on 19 Apr 2021
Print article
Image: Qorvo Omnia SARS-CoV-2 Antigen Test (Photo courtesy of Qorvo Biotechnologies, LLC)
Image: Qorvo Omnia SARS-CoV-2 Antigen Test (Photo courtesy of Qorvo Biotechnologies, LLC)
A new COVID-19 test platform represents a paradigm shift in diagnostic testing capability by using high frequency Bulk Acoustic Wave (BAW) sensors to achieve SARS-CoV-2 antigen testing in approximately 20 minutes.

Qorvo Biotechnologies, LLC (Greensboro, NC, USA) has been granted emergency use authorization (EUA) by the U.S. Food and Drug Administration (FDA) for its Qorvo Omnia SARS-CoV-2 Antigen Test. The test is authorized for the qualitative detection of nucleocapsid viral antigens from SARS-CoV-2 in nasal swab specimens from individuals who are suspected of COVID-19.

The Qorvo Omnia platform features a portable test instrument, microfluidic cartridge and secure connectivity. The microfluidic cartridge design enables specific binding with additional wash steps similar to central lab instrument operation and demonstrated results including 100% specificity during clinical trials. BAW sensor technology enables low Limit of Detection (LOD) levels that are similar to molecular testing capability.

“This is very exciting news. FDA authorization of Qorvo’s Omnia Antigen Test provides a rapid, sensitive and specific assessment of individuals, assisting providers trying to either rule in or rule out COVID-19, comparable to many of the PCR testing platforms in use,” said Fred S. Apple, Ph.D., a member of Qorvo Biotechnologies’ advisory board, Co-Medical Director of Toxicology Laboratory at Hennepin Healthcare/Hennepin County Medical Center, and Professor of Laboratory Medicine & Pathology at the University of Minnesota. “The testing system will hopefully be an avenue to assist in opening up the United States to be closer to business as usual.”

“The FDA’s EUA is recognition that the Qorvo Omnia platform can help address the ongoing need for rapid, accurate and clinically-reliable diagnostic testing,” added James Klein, President of Qorvo Biotechnologies. “We are honored to leverage Qorvo’s technology portfolio to help public health officials respond to this global pandemic.”

Related Links:
Qorvo Biotechnologies, LLC

New
Gold Supplier
COVID-19 Neutralization Antibody Test
iFlash-2019-nCoV Neutralization Antibody Test
New
COVID-19 Antigen Rapid Test
OnSite COVID-19 Ab Rapid Test
New
Gold Supplier
COVID-19 Nucleic Acid Releaser (For PCR)
Nucleic Acid Releaser (For PCR)
New
Gold Supplier
Molecular & Immunoassay Diagnostic Analyzer
Randox Discovery

Print article
BIOHIT  Healthcare OY
Mayo Medical Laboratories

Channels

Pathology

view channel
Image: The Hamamatsu Photonics Nanozoomer 1 Digital Slide Scanner (Photo courtesy of University of Adelaide)

Genetic Background and Clinicopathologic Features Established for Adult-Onset Nephronophthisis

Nephronophthisis (NPH) is a genetic disorder of the kidneys which mainly affects children. It is classified as a medullary cystic kidney disease. The disorder is inherited in an autosomal recessive fashion... Read more

Industry

view channel
Image: DxA 5000 Fit (Photo courtesy of Beckman Coulter)

Beckman Coulter Becomes First Diagnostics Company to Offer Workflow Automation Specifically for Mid-Volume Laboratories

Beckman Coulter (Brea, CA, USA) has announced the global launch of the DxA 5000 Fit, a workflow-automation solution designed to fit into medium-sized labs that run fewer than 5,000 tests a day.... Read more
Copyright © 2000-2021 Globetech Media. All rights reserved.