Nkhani - FDA imavomereza kuyesa koyamba kwa COVID-19 kunyumba popanda kulembedwa ndi dokotala

Bungwe la Food and Drug Administration dzulo lidavomereza LabCorp's Pixel COVID-19 Test Home Collection Kit kuti igwiritsidwe ntchito ndi akuluakulu popanda kulembedwa.A FDA adawunikiranso ndikuperekanso chilolezo chogwiritsa ntchito mwadzidzidzi pakuyezetsako kuti alole munthu kutolera mphuno kunyumba ndikutumiza ku LabCorp kuti akayezedwe, ndi zotsatira zabwino kapena zosavomerezeka zoperekedwa ndi wothandizira zaumoyo pafoni ndi zotsatira zoyipa zomwe zimaperekedwa kudzera pa imelo. kapena portal yapaintaneti.

"Ngakhale zida zambiri zosonkhanitsira kunyumba zitha kulembedwa ndi mafunso osavuta a pa intaneti, zida zomwe zangololedwa kumenezi zimachotsa zomwe zikuchitika, kulola aliyense kutenga zitsanzo zake ndikuzitumiza ku labu kuti akakonze," adatero Jeff. Shuren, MD, mkulu wa FDA's Center for Devices and Radiological Health.