Latest Headlines
-
YD Bio And EG BioMed Expand U.S. Access To OkaiDx™, A cfDNA Methylation Blood Test For Post Treatment Breast Cancer Monitoring
11/5/2025
YD Bio Limited (“YD Bio” or the “Company”) (NasdaqGM: YDES), a biotechnology company advancing DNA methylation-based cancer detection technology and ophthalmologic innovations, today announced its support for the global commercialization of OkaiDx™, a research‑use‑only (RUO) blood test for post‑treatment breast cancer monitoring now available through the Company’s affiliate EG Biomed US Inc.
-
Illumina And Grail Veterans Launch Hepta With First Liquid Biopsy-Native AI That Detects Liver Disease With Tissue-Level Biological Insights
11/5/2025
Hepta, a biotechnology company using transformer-based AI to read the cell-free DNA (cfDNA) epigenome and detect organ-specific signals of chronic disease, today emerged from stealth with $6.7M in seed funding led by Felicis Ventures and Illumina Ventures, with participation from SeaX Ventures, Alumni Ventures, and AME Cloud Ventures.
-
QIAGEN To Acquire Parse Biosciences, Expanding Its Sample Technologies Portfolio Into Highly Scalable Single-Cell Solutions
11/4/2025
QIAGEN today announced it has entered into a definitive agreement to fully acquire Parse Biosciences, a leading provider of scalable, instrument-free solutions for single-cell research.
-
Countable Labs Announces Additional Modules For Countable PCR Expanding Its Utility For Translational Research, Cell And Gene Therapy Manufacturing, And Diagnostic Development
11/4/2025
Countable Labs, the developer of Countable PCR, the leading PCR innovation transforming how science measures biology, announced the launch of the RNA Module for Countable PCR.
-
SimplyTest Partners With Evexia Diagnostics To Expand Access To PERIO And 4-Point Cortisol Tests For Functional And Integrative Health Practitioners
11/4/2025
SimplyTest is proud to announce a new partnership with Evexia Diagnostics, a premier provider of diagnostic laboratory services for functional and integrative medicine.
-
QuidelOrtho Receives FDA 510(k) Clearance For VITROS™ Immunodiagnostic Products hs Troponin I Assay
11/3/2025
The U.S. Food and Drug Administration ("FDA") has granted QuidelOrtho Corporation (Nasdaq: QDEL) ("QuidelOrtho"), a global leader of in vitro diagnostics, 510(k) clearance for the VITROS hs Troponin I Reagent Pack (the "VITROS hs Troponin I Assay").
-
Co-Diagnostics To Integrate And Implement Proprietary Artificial Intelligence Technology Into Co-Dx™ Primer Ai™ Platform
11/3/2025
Co-Diagnostics, Inc. (Nasdaq: CODX) (the "Company" or "Co-Dx"), a molecular diagnostics company with a unique, patented platform for the development of molecular diagnostic tests, today announced the formation of a newly organized, artificial intelligence ("AI") business unit, led by Chief Technology & AI Officer Christopher Thurston, to integrate the Company's existing and planned AI applications into the Co-Dx™ Primer Ai™ platform.
-
AIxMed And PathNet Partnership: Advancing Digital Pathology With AI-Powered Urine Cytology
11/3/2025
AIxMed, a recognized innovator in AI diagnostics for urine cytology, and PathNet, a leading diagnostic laboratory, announced a strategic partnership.
-
First In The United States To Offer New Testicular Cancer Blood Test
11/3/2025
UC San Diego Health is the first health system in the country to offer a new blood test for testicular cancer, a major advancement in the treatment and surveillance of patients with the disease.
-
BD Receives FDA 510(k) Clearance And CE-IVDR Certification For High-Throughput Enteric Bacterial Panels On BD COR™ System
11/3/2025
BD (Becton, Dickinson and Company) (NYSE: BDX) a leading global medical technology company, today announced it has received U.S. Food and Drug Administration (FDA) 510(k) clearance and Conformité Européenne (CE) marking in the European Union for its Enteric Bacterial Panel* (EBP) and Enteric Bacterial Panel plus* (EBP plus) for the BD COR™ System.