F.D.A. Advisory Panel Recommends Approval Of Simple H.I.V. Home Test
Giving themselves a simple and rapid test for the Human immunodeficiency virus (HIV) causing AIDS may soon be possible for Americans, as a panel of the experts recommended the approval of the first rapid test for HIV on Tuesday.
The advisory panel included 17 members of the Food and Drug Administration. In a unanimous vote, the advisory panel of experts decided that the OraQuick H.I.V. test’s advantages overshadow the potential risk of HIV for consumers. The test returns result in 20 minutes using a mouth swab. However, the test result does not appear to be accurate like professionally administered diagnostics. This year, the Food and Drug Administration will take a stand on whether to approve the product or not.
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