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Roche's new rapid STI test gets FDA approval, speeding up diagnosis and treatment in urgent care settings.
Roche has received FDA clearance for its cobas® liat STI test, allowing point-of-care diagnosis of infections like chlamydia and gonorrhea in settings such as urgent care and retail clinics.
The test, which provides results in 20 minutes, aims to improve access to accurate diagnostics and reduce the spread of STIs.
Initially available in the U.S., it will help in faster treatment and better health outcomes.
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La nueva prueba rápida de STI de Roche recibe la aprobación de la FDA, acelerando el diagnóstico y el tratamiento en entornos de atención urgente.