The FDA has been timid on COVID tests. It should have been bold.

A home COVID test kit in the U.K.
(Image credit: BEN STANSALL/AFP/Getty Images)

One of the more aggravating aspects of the Omicron surge is that the country needs lots and lots of COVID tests, preferably cheap, but getting them is difficult. It's easier to slow the spread of a virus — or to safely visit family at the holidays — if you know who has the bug and who doesn't. But nearly two years into the pandemic, achieving that simple goal in America is still elusive. (In Europe, testing kits are relatively cheap and easy to obtain.)

The problem seems to be at the FDA. ProPublica reported last month that companies trying to develop rapid COVID tests have encountered an "arbitrary, opaque process" which takes so long to complete that one agency scientist quit in frustration earlier this year. One company was ready to roll out a product in March 2020, right as the pandemic was getting under way, but approval never came.

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Joel Mathis, The Week US

Joel Mathis is a writer with 30 years of newspaper and online journalism experience. His work also regularly appears in National Geographic and The Kansas City Star. His awards include best online commentary at the Online News Association and (twice) at the City and Regional Magazine Association.