The US Food and Drug Administration (FDA) has cleared the cobas Influenza A/B test for use on the cobas Liat System, according to manufacturer Roche. It is the first Clinical Laboratory Improvement ...
It uses standard, real-time PCR, requires no technical expertise and delivers battery-powered, sample-to-answer results within one hour, without the need to mail in a sample. The Nuclein Hand-Held PCR ...
Two-hour test is more sensitive than direct culture-based methods, firm claims. FDA cleared Roche Molecular Systems’ LightCycler® MRSA Advanced Test for detecting methicillin-resistant Staphylococcus ...
As part of ongoing efforts to enhance quality-assured testing options, the World Health Organization (WHO) has listed two additional mpox in vitro diagnostics under its Emergency Use Listing (EUL) ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback