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Ubiquitome Gets FDA Authorization with Yale COVID Self-Collection Tests

Posted by Andy Lundin | Dec 19, 2022 | Covid 19 |

Ubiquitome’s next generation real-time PCR device system, the Liberty16 Pro, has been given Emergency Use Approval (EUA) by the FDA.

The FDA granted Emergency Use Authorization (EUA) for Thermo Fisher Scientific’s Applied Biosystems TaqPath Monkeypox/Orthopox Virus DNA Kit.

Two out of three Americans are confused by the differences between polymerase chain reaction, or PCR, tests, and rapid antigen tests.

Sameday Health launched a single swab test for COVID, influenza A/B strains, and respiratory syncytial virus (RSV).

Posted by Andy Lundin | Dec 16, 2022 | Covid 19 |

A team of researchers developed the Quenchbody fluorescent immunosensor, which can detect COVID with exceptional speed and sensitivity.