Get all your news in one place.
100’s of premium titles.
One app.
Start reading
Axios
Axios
Health

FDA authorizes emergency use for first coronavirus antigen test

The Food and Drug Administration on Friday authorized a new coronavirus antigen test produced by Quidel Corporation, a California-based diagnostic testing company.

Why it matters: Antigen tests deliver results quickly and are relatively easy to produce, though their results are less accurate than the standard tests the U.S. has been using so far.


What's happening: “We are ramping up manufacturing to go from 200,000 tests next week [week of May 11] to more than a million a week within several weeks,” Douglas Bryant, Quidel’s CEO, told the Wall Street Journal.

  • Quidel has currently provided roughly 36,000 "test-analyzer instruments" in doctors' offices and hospitals, per the WSJ.

Between the lines: Antigen tests create a greater chance of false negatives, CNBC reports, and a negative antigen result may need to be confirmed with additional testing. But, positive antigen test results are usually highly accurate.

The big picture: The U.S. will need coronavirus tests that can detect antigens, or the part of a pathogen that triggers an immune response, as part of a testing breakthrough needed to screen a large number of people for the virus, Deborah Birx, White House coronavirus task force coordinator, said in April.

Go deeper: Coronavirus testing increasing, but still not good enough

Sign up to read this article
Read news from 100’s of titles, curated specifically for you.
Already a member? Sign in here
Related Stories
Top stories on inkl right now
Our Picks
Fourteen days free
Download the app
One app. One membership.
100+ trusted global sources.