TSXV:SQD.H - Post by User
Comment by
ResearchGuyon Oct 26, 2020 7:50am
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Post# 31780205
RE:News is Out
RE:News is Out"highlighted by confirmation from the U.S. FDA that Emergency Use Authorization (EUA) submission is acceptable for all three COVID diagnostic tests. SQI is accelerating the clinical development of its direct-to-consumer COVID-19 HOME Antibody Test, its COVID-19 RALI-dx ™ Severity Triage Test and its COVID-19 RALI- fast ™ Severity Triage Point-of-Care (POC) Test."