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FDA approves at-home sample collection kit for coronavirus

WASHINGTON, D.C. – The Food and Drug Administration announced Saturday that it has authorized an at-home sample collection kit that can then be sent to specified laboratories for COVID-19 diagnostic ...
RAPS

FDA issues EUA for saliva-based COVID-19 test, provides path for wider home sample collection

FDA issues EUA for saliva-based COVID-19 test, provides path for wider home sample collection The US Food and Drug Administration (FDA) on Friday granted the first emergency use authorization (EUA) ...
RAPS

FDA releases EUA template for COVID-19 home sample collection kits

The US Food and Drug Administration (FDA) on Friday released a new emergency use authorization (EUA) template to assist test makers in developing at-home sample collection kits for use with tests for ...
Business Wire

Rheonix COVID-19™ MDx Assay Receives Expanded FDA Emergency Use Authorization to Include Saliva Home Collection Kit

ITHACA, N.Y.--(BUSINESS WIRE)--Rheonix Inc. announced today that the United States Food and Drug Administration (FDA) has issued an expanded Emergency Use Authorization (EUA) for the Rheonix COVID-19™ ...
WRAL

Collection method, sample timing can impact COVID-19 test results

1.2 million COVID-19 tests have been completed across the state and counting. 87,000 of those tests are confirmed positive. Are results from a drive-thru "self" tests as reliable as those from a ...
Business Wire

University Medical Devices Launches First-of-its-Kind Nasal Lavage Specimen Collection Device to Provide Healthcare Organizations With Faster, Higher-Sensitivity Samples

OMAHA, Neb.--(BUSINESS WIRE)--University Medical Devices (UMD), a cutting-edge healthcare technology developer, today announced the launch of its first specimen collection method, MicroWash. Developed ...