Against the background of an increasingly aging global population, the incidence of thrombotic and hemostatic diseases, including cardiovascular diseases, remains high.

Stay up-to-date with the latest happenings in the rapidly evolving field of In Vitro Diagnostics (IVD) in China.

Co-Diagnostics has been part of the coronavirus conversation for the past two months. Whether its been educating the public about the disease or developing diagnostics for the virus, the company has been at the forefront. Now the Salt Lake

Reorg Research reported that Medtronic is in early-stage acquisition talks withLivaNova, news that has been well received by LivaNova shareholders. The firm said Medtronic would subsequently break up LivaNova, keeping its neuromodulation bu

FDA is upping its response to address the novel coronavirus outbreak. The policy is aimed at laboratories seeking to develop diagnostic tests for the coronavirus. The policy allows laboratories to develop and begin to use the diagnostics be

Quest Diagnostics joins the growing number of firms that have developed tests for the coronavirus (COVID-19) in recent weeks.The Secaucus, NJ-based company said it was launching its COVID-19 test service that aids in the presumptive detecti

NEW YORK The US Food and Drug Administration on Friday granted Emergency Use Authorization to Luminex for the firms NxTag CoV Extended Panel to detect SARS-CoV-2 virus nucleic acids in nasopharyngeal swab specimens. High-complexity molecula

NEW YORK Avellino Labs on March 25 received Emergency Use Authorization for its coronavirus real-time PCR diagnostic test from the US Food and Drug Administration. The assay, called AvellinoCoV2 test, is designed for the detection of nuclei

NEW YORK Sysmex said Friday it has obtained marketing approval in Japan for the distribution of BGI Genomics 2019-nCoV Fluorescence Detection Real-Time RT-PCR Kit. Financial and other terms of the agreement were not disclosed. Sysmex said t

NEW YORK Fosun Pharmaceutical said on Thursday that its Fosun Long March Medical Science subsidiary has received emergency approval from Chinas National Medical Products Administration for a SARS-CoV-2 detection kit. According to Shanghai,

New York PerkinElmer said after the close of the market on Tuesday that the US Food and Drug Administration has issued Emergency Use Authorization for the firms coronavirus RT-PCR test. CLIA-certified labs can immediately use the PerkinElme

NEW YORK Mesa Biotech said on Tuesday that it has received Emergency Use Authorization from the US Food and Drug Administration for its Accula SARS-CoV-2 test. The PCR test is designed for the qualitative visual detection of nucleic acid fr