Post by
ResearchGuy on Oct 26, 2020 7:47am
News is Out
The news is out let's see if we have an amazing day!!!!
Comment by
ResearchGuy on Oct 26, 2020 7:50am
"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."
Comment by
ResearchGuy on Oct 26, 2020 8:01am
I am sure the application process for Emergency use will not take long.