Recently AmoyDx ROS1 gene fusion detection kit (fluorescence PCR method) was approved by Taiwan Food and Drug Administration（TFDA).

Foundation Medicine announced recently that its FoundationOne CDx genomic profiling assay has received regulatory approval from Japan's Ministry of Health, Labour and Welfare (MHLW).

Cepheid announced recently it has received CE-IVD clearance for a rapid molecular assay to measure viral load of hepatitis B in infected patients.

French diagnostics firm Novacyt announced recently that it has received CE marking for its Genesig BK virus (BKV) and Epstein-Barr virus (EBV) diagnostic kits, which are designed for use in post-transplantation and immunosuppressed patients.

Imagine being a pediatric kidney transplant patient and having to miss school or extracurricular activities because of clinic appointments and routine blood tests.

At the close of the 2014-2016 West Africa Ebola crisis, the Paul G. Allen Foundation identified diagnostic gaps as one of the major deficiencies that had contributed to the outbreak’s spread.

Brigham and Women’s Hospital investigators are working on a test that could either diagnose or predict Alzheimer’s disease before symptoms appear.

A long-awaited and massive study with major implications for the liquid biopsy market is slated to start next year.

Oxford HighQ has received ￡2.1 million in seed funding to commercialize components of a quantum computing technology developed at Oxford University that can be used to develop improved chemical and nanoparticle sensing technologies.

An innovative new medical instrumentation and biotechnology company known as Daxor just published some exciting new data for their flagship technology, the BVA-100 blood volume analyzer.

A cell-by-cell search for cardiac stem cells has come up empty, suggesting that previous studies hinting at the existence of cardiac stem cells were mistaken.

Biocartis announced it has entered into an agreement with AstraZeneca.

Agilent technologies has announced a new expansion of its Little Island facility in cork, Ireland.

Mesa Biotech recently said that the US Food and Drug Administration has cleared and CLIA-waived the company's Accula RSV respiratory syncytial virus test for diagnostic use in both children and adults.

Novacyt announced recently that its molecular testing division, Primerdesign, has inked an exclusive supply agreement with Genesis Diagnostics.