What Next TBD: Are We Getting COVID Testing All Wrong?
Slate Technology
00:00
The Fda Is Changing the Goald Posts on Us
The fda defines the tests as medical vices. They want rapid antegen tests to show sensitivity comparable to pc r tests. Only a handful of companies met that requirement and could get emergency use authorization for their tests. Other companies have the technology, but not the authorization. It just feels like the fda is like changing the goald posts on us," he says.
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