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FDA approves first at-home test for three common STIs, aimed at increasing diagnosis rates.
The FDA has authorized the first at-home test for detecting chlamydia, gonorrhea, and trichomoniasis, developed by Visby Medical.
This test, intended for women, provides results in about 30 minutes without requiring a prescription or lab processing.
By making STI testing more accessible, the FDA aims to increase diagnosis and treatment rates, potentially reducing the spread of these infections.
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La FDA aprueba la primera prueba en casa para tres ITS comunes, con el objetivo de aumentar las tasas de diagnóstico.