Different medical institutions have selected different imported and domestic brand instruments: 38 domestic and 58 imported.

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

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.

Roche said on Friday that it has acquired Seattle-based early-stage sequencing technology firm Stratos Genomics for an undisclosed amount in a bid to advance development of Roche's nanopore sequencer.

Regeneron Pharmaceuticals and the Colorado Center for Personalized Medicine (CCPM) said Monday that they would sequence 450,000 exomes and match the results with phenotypic data from deidentified patient health records to advance drug discov

Quanterix said on Monday it has inked a non-exclusive agreement with Brigham and Women's Hospital for a SARS-CoV-2 serology test on its Simoa multiplex immunoassay platform.