The test is now authorized for use with anterior nasal swab samples in addition to the previously authorized throat and nasopharyngeal samples.

Last week, readers were most interested in a story about WHO's update to its operational handbook for diagnosing tuberculosis.

The submission releases $1.3 million in US funding support from the Biomedical Advanced Research and Development Authority (BARDA), the firm said.

TBI is a potential new application area for the 8-year-old company, while it continues to commercialize its stroke triage ...

The company's Acute Respiratory Distress and Pneumonia test is a PCR-based assay for the detection and differentiation of about 100 causes of infections.

The firm said that it will use the money for working capital and general corporate purposes, and the raise follows a $3.25 million public offering that closed in May.

The firm's goal for its SeekIt platform is to combine the accessibility of antibody and antigen testing and the accuracy of PCR for use in low-resource settings.

Genco Lab was accused of billing Medicaid and Medicare programs for unnecessary screening and confirmatory tests for the use of prohibited drugs.

The US Food and Drug Administration granted clearances for PCR-based infectious disease tests from multiple entities as well as other in vitro diagnostic tests.

The technology can more effectively test for antibiotic susceptibility in heteroresistant bacterial populations than existing approaches.

NEW YORK – The US Court of Appeals for the Federal Circuit on Wednesday reversed a patent infringement jury verdict against Qiagen related to DNA sequencing sample preparations methods. Four years ago ...