A meeting report details how open PCR platforms and reagents can sustain national molecular diagnostic networks beyond ...
EVANSTON, Ill.--(BUSINESS WIRE)--Minute Molecular Diagnostics today announced that the U.S. Food and Drug Administration (FDA) granted an Emergency Use Authorization (EUA) for its rapid DASH ...
Home diagnostics company Cue Health announced its received FDA de novo authorization for its at-home COVID-19 test, dubbed the Cue COVID-19 Molecular Test. The Cue COVID-19 Molecular Test detects ...
The FDA has issued its first emergency use authorization for a COVID-19 molecular diagnostic test that does not require a prescription and can be used at home. Developed by Cue Health, the Cue ...
Explore the evolving role of respiratory viral testing after COVID-19 and how test results guide patient care, treatment decisions, and efficiency.
TIB MOLBIOL’s products are being used in a number of fields such as life science research, medical diagnostics, product quality assessment and environmental analysis. To help businesses overcome ...