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Different medical institutions have selected different imported and domestic brand instruments: 38 domestic and 58 imported.
P23 Labs has received Emergency Use Authorization for its coronavirus PCR test from the US Food and Drug Administration.
The US Food and Drug Administration on Thursday granted separate Emergency Use Authorizations (EUAs) for PCR-based SARS-CoV-2 tests developed by South Korean diagnostic test makers BioCore, SolGent, and Seasun Biomaterials.
Agilent Technologies reported after the close of the market on Thursday that its second quarter 2020 revenue growth was flat year over year. The firm noted that core revenues, which excludes the impact of currency and acquisitions and divest
The US Food and Drug Administration on Wednesday announced the approval of AstraZeneca and Merck's olaparib (Lynparza) for metastatic castration-resistant prostate cancer patients with homologous recombination repair deficiency.
Proteomics firm Nautilus Biotechnology announced Thursday it has closed an oversubscribed $76 million Series B financing round.
Northern and southern Italian populations began to diverge genetically thousands of years ago, according to a new study.
P23 Labs has received Emergency Use Authorization for its coronavirus PCR test from the US Food and Drug Administration.
The US Food and Drug Administration on Thursday granted separate Emergency Use Authorizations (EUAs) for PCR-based SARS-CoV-2 tests developed by South Korean diagnostic test makers BioCore, SolGent, and Seasun Biomaterials.
Tony Serafini-Lamanna, Martin Chavez, Sun Kim, Oved Amitay, More
Host factors rather than viral genetic differences appear to influence disease outcomes among COVID-19 patients, according to a new study from China.
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