Home

Articles from MeMed

MeMed BV Surpasses 100,000 Patient Tests, Underscoring Adoption of Rapid Host-Response Diagnostics
MeMed, a global leader in host-response diagnostics, today announced a major milestone: more than 100,000 patients have now been tested with MeMed BV®, the company’s flagship diagnostic that accurately distinguishes between bacterial and viral infections in just 15 minutes, based on the body’s immune response. This milestone highlights MeMed’s commitment to advancing precision medicine, empowering responsible antibiotic use by care providers, and transforming infection management across diverse care settings.
By MeMed · Via Business Wire · June 5, 2025
MeMed BV Proven to Optimize Antibiotic Use, Outperform Standard Care, and Cut Costs in New Studies
MeMed, a leader in host-response diagnostics, today announced the publication of three new peer-reviewed studies, reinforcing the real-world clinical and economic impact of MeMed BV, its flagship diagnostic for differentiating between bacterial and viral infections. Conducted across multiple centers in the U.S., Europe, and the U.K., and involving thousands of patients, these independent studies highlight distinct aspects of MeMed BV’s impact, including better antibiotic stewardship, superior performance over the standard of care, and reduced healthcare costs.
By MeMed · Via Business Wire · February 27, 2025
MeMed Expands Advisory Board with Key Leaders to Advance Host-Response Diagnostics for Sepsis and AMR
MeMed, a leader in host-response diagnostics, today announced the addition of three distinguished experts to its advisory board to accelerate its mission of addressing the global challenges of sepsis and antimicrobial resistance (AMR) through innovative diagnostic solutions. These new members bring decades of experience in medicine, industry, and healthcare policy, strengthening MeMed’s work in host-response technologies, which combine machine learning with rapid measurements of the immune response to transform infectious disease care.
By MeMed · Via Business Wire · January 9, 2025
FDA Grants Breakthrough Device Designation to MeMed Severity Test for Patients with Suspected Sepsis
MeMed, a leader in the emerging field of advanced host response technologies, today announced that the FDA has granted Breakthrough Device Designation (BDD) to its innovative MeMed Severity™ test. This designation underscores the transformative potential of MeMed Severity to advance the management of patients with suspected acute infections and suspected sepsis by empowering clinicians with timely, data-driven, clinical insights.
By MeMed · Via Business Wire · December 10, 2024
MeMed awarded US BARDA contract to demonstrate clinical utility of the FDA-cleared MeMed BV® test for distinguishing bacterial from viral infections
Contract awarded under the BARDA DRIVe (Division of Research, Innovation, and Ventures) initiative to harness a patient's systemic response to inform on health threats and clinical impact
By MeMed · Via GlobeNewswire · October 24, 2023
MeMed: FDA Clears Pioneering MeMed BV Test Direct From Whole Blood Allowing Faster Time To Result And Broader Patient Access When Distinguishing Bacterial From Viral Infections
FDA Clears Pioneering MeMed BV Test Direct From Whole Blood Allowing Faster Time To Result And Broader Patient Access When Distinguishing Bacterial From Viral Infections
By MeMed · Via GlobeNewswire · July 19, 2023