USFDA clears basic salivation test for quicker identification of COVID-19 Kumar Jeetendra | August 16, 2020 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 Kumar Jeetendra | April 13, 2021 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 …
