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    • Roche gets USFDA...

    Roche gets USFDA Emergency Use Authorization for its Cobas SARS-CoV-2 Test

    Medical Dialogues BureauWritten by Medical Dialogues Bureau Published On 2020-03-15T12:49:39+05:30  |  Updated On 15 March 2020 12:49 PM IST
    Roche gets USFDA Emergency Use Authorization for its Cobas SARS-CoV-2 Test

    Basel: Roche has announced that the U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for the cobas® SARS-CoV-2 Test. It is intended for the qualitative detection of SARS-CoV-2, the virus that causes COVID-19 disease, in nasopharyngeal and oropharyngeal swab samples from patients who meet COVID-19 clinical and/or epidemiological criteria for testing. Hospitals and reference laboratories can run the test on Roche's fully automated cobas® 6800 and cobas® 8800 Systems, which are widely available in the U.S. and around the world.

    The CE-IVD test is also available in markets accepting the CE mark for patients with signs and symptoms of COVID-19 disease and living in affected areas where the SARS-CoV-2 virus is known to be present.

    "Providing quality, high-volume testing capabilities will allow us to respond effectively to what the World Health Organization has characterized as a pandemic. It is important to quickly and reliably detect whether a patient is infected with SARS-CoV-2," said Thomas Schinecker, CEO of Roche Diagnostics. "Over the last weeks, our emergency response teams have been working hard to bring this test to the patients. CE-mark certification and the FDA's granting of EUA supports our commitment to give more patients access to reliable diagnostics which are crucial to combat this serious disease."

    The widely available Roche's Cobas 6800/8800 Systems, which are used to perform the cobas SARS-CoV-2 Test, provide test results in three and half hours and offer improved operating efficiency, flexibility, and fastest time-to-results with the highest throughput providing up to 96 results in about three hours and a total of 1,440 results for the cobas 6800 System and 4,128 results for the cobas 8800 System in 24 hours. The test can be run simultaneously with other assays provided by Roche for use on the cobas 6800/8800 Systems.

    Upon authorisation, Roche will have millions of tests a month available for use on the Cobas 6800 and 8800 systems. Roche is committed to delivering as many tests as possible and is going to the limits of our production capacity.

    Read also: Roche Gets USFDA Nod For CINtec PLUS Cytology Test For Cervical Cancer

    rochecoronaviruscovid-19usfdathomas-schineckercoronavirus test

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    Medical Dialogues Bureau
    Medical Dialogues Bureau

      Medical Dialogues Bureau consists of a team of passionate medical/scientific writers, led by doctors and healthcare researchers.  Our team efforts to bring you updated and timely news about the important happenings of the medical and healthcare sector. Our editorial team can be reached at editorial@medicaldialogues.in. Check out more about our bureau/team here

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