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    Saliva Test

    USFDA clears basic salivation test for quicker identification of COVID-19

    Houston, Aug 16 (PTI) The US health watchdog has authorised the emergency use of some new and expensive saliva established laboratory diagnostic test for COVID-19 which might be a game changer in the identification of the infection because it will enable rapid testing among more people easily. Stephen Hahn, the Food and Drugs Administration Commissioner,

    AnteoTech Secures CE Certification for Its Versatile EuGeni™ Rapid Diagnostic Platform

    Brisbane, AUS, April 13, 2021 – AnteoTech has announced that its EuGeni™ Reader and accompanying COVID-19 Antigen Rapid Test (ART) have received Conformité Européene (CE) Mark registration as the company looks to progress with European distribution. The digital multi-test EuGeni Reader eliminates the human error associated with current lateral flow test interpretation, and can support