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Investegate |Omega Diagnostics Gp Announcements | Omega Diagnostics Gp: FDA submission for Emergency Use Authorization

Investegate |Omega Diagnostics Gp Announcements | Omega Diagnostics Gp: FDA submission for Emergency Use Authorization
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Omega Diagnostics Group partner files FDA request for emergency approval of Covid-19 antigen test | 2 July 2021

Omega Diagnostics Group partner files FDA request for emergency approval of Covid-19 antigen test | 2 July 2021
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Today s Market View - All Active Asset Capital, Distribution Finance, E-therapeutics and more

Today s Market View - All Active Asset Capital, Distribution Finance, E-therapeutics and more
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LivFul and Global Access Diagnostics announce partnership for COVID-19 test kit distribution

Avacta Receives Clinical Validation of AffiDX SARS-CoV-2 Antigen Lateral Flow Test

Avacta Receives Clinical Validation of AffiDX SARS-CoV-2 Antigen Lateral Flow Test 1 up to 31 in early May, followed immediately by commercial launch in Europe Avacta Group plc (AIM: AVCT), the developer of diagnostics and innovative cancer therapies based on its proprietary Affimer and pre|CISION platforms, is pleased to announce positive data from the clinical validation of its AffiDX SARS-CoV-2 antigen lateral flow test. Data from the clinical study conducted in Europe on 98 positive COVID-19 samples demonstrate excellent performance in identifying the SARS-CoV-2 virus across a broad range of viral loads. These data will now be combined with stability and other performance data from ongoing studies to finalise the technical file for CE marking the AffiDX SARS-CoV-2 antigen lateral flow test for professional use, allowing the Company to begin commercial roll-out in Europe in May.

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