MERS Diagnostic Test Gains Emergency Approval From FDA

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The U.S. Food and Drug Administration issued an emergency authorization on Tuesday for a diagnostic test to detect the presence of the Middle East coronavirus at the request of the Centers for Disease Control and Prevention. The emergency approval follows the Health and Human Services secretary’s determination that the virus called Middle East Respiratory Syndrome Coronavirus (MERS-CoV), which has killed at least 40 people, poses a potential public health threat.

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