Dr. Henry Miller, M.S., M.D., joins the nationally-syndicated Lars Larson Show to talk about how the U.S. Food and Drug Administration, FDA, blocked a crucial test, the rapid response antigen test, to help with COVID-19 testing.
The test is an at-home test that takes roughly 20 minutes. Dr. Miller explains that the test is considered a medical device because of the vague rules around regulations and the strict regulations mean the test, which could be effective for rapid testing, is more expensive.
