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BioWorld - Friday, February 6, 2026
Home » Authors » Meg Bryant

Articles by Meg Bryant

BioWorld MedTech’s Diagnostics Extra for April 23, 2020

April 23, 2020
By Meg Bryant and Anette Breindl
Keeping you up to date on recent developments in diagnostics, including: Automated CT biomarkers predict future CV events; PCR heightens detection of scabies; High BMI linked to dementia via complement component.
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Study to evaluate benefit of Cardiologs’ AI-based tool in monitoring COVID-19 patients

April 22, 2020
By Meg Bryant
Paris-based health care startup Cardiologs Technologies SAS has launched a clinical study to assess the use of its artificial intelligence (AI) platform to remotely monitor cardiac safety in COVID-19 patients being treated with the malaria drug hydroxychloroquine. The study could help to detect and prevent serious cardiac effects of the drug.
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Artificial retina program wins $5M NASA award

April 21, 2020
By Meg Bryant
Farmington, Conn.-based biotech startup Lambdavision Inc. is preparing to test the benefits of microgravity in producing its protein-based artificial retina, thanks to a $5 million, three-year award from the National Aeronautics and Space Administration (NASA). The first-of-a-kind treatment aims to restore vision to people who have lost all or much of their sight due to advanced retinitis pigmentosa (RP).
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Vent Multiplexor’s ventilator-sharing device wins FDA nod for emergency use

April 20, 2020
By Meg Bryant
The U.S. FDA has granted emergency use authorization (EUA) to New Haven, Conn., startup Vent Multiplexor LLC for its emergency rescue co-ventilation device. Developed in collaboration with Yale New Haven Hospital, the Vent Multiplexor enables individualized mechanical ventilation of two adults on a single ventilator – lessening demand for more critical care machines in the ongoing COVID-19 outbreak.
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Dollar sign in lightbulb

Hememics’ rapid point-of-care COVID-19 test gets infusion from BARDA

April 16, 2020
By Meg Bryant
Gaithersburg, Md.-based startup Hememics Biotechnologies Inc. is partnering with the U.S. Biomedical Advanced Research and Development Authority (BARDA) to develop a rapid, Bluetooth-connected, point-of-care (POC) test for COVID-19. Designed for use in both field and traditional settings, the test detects SARS-CoV-2 and related antibodies from nasal swabs and whole blood, delivering results in a minute or less.
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BioWorld MedTech’s Diagnostics Extra for April 16, 2020

April 16, 2020
By Meg Bryant
Keeping you up to date on recent developments in diagnostics, including: CEUS LI-RADS for diagnosing liver cancer; Variations in echocardiography recommendations for patients with S. aureus; Reusable bronchoscopes and COVID-19 patients.
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COVID-19, coronavirus paper dolls

Mass fever scanner could reduce spread of COVID-19

April 15, 2020
By Meg Bryant
As state and federal authorities deliberate over how to safely reopen U.S. society during the ongoing COVID-19 pandemic, tools that effectively monitor body temperature at a population level could help to get the ball rolling. To that end, software development firm Altoros Inc., of Sunnyvale, Calif., has released the Fever Screener, a fully automated, enterprise-grade system for setting up temperature scanning checkpoints. Fever Screener can scan up to 30 people simultaneously at a distance of 3 meters, or nearly 10 feet, with a temperature accuracy of roughly 0.6 degrees Fahrenheit. Installed in entryways, checkpoints or other crowded venues, it can provide mass screenings, as well as recurrent temperature monitoring for potentially infected individuals.
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FDA greenlights Tack endovascular system for below-the-knee intervention

April 14, 2020
By Meg Bryant
Wayne, Pa.-based Intact Vascular Inc. has secured U.S. FDA approval for the first peripheral vascular implant to repair below-the-knee (BTK) post-angioplasty dissections. The company expects to begin shipping units of the Tack endovascular system (4F) in about two weeks.
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Stony Brook, Chembio Diagnostics partner on COVID-19 trial

April 13, 2020
By Meg Bryant
Stony Brook Medicine has launched an FDA-approved, randomized investigational new drug (IND) trial to determine whether plasma from people who have recovered from COVID-19 can aid in the recovery of patients currently fighting the disease. Chembio Diagnostics Inc.'s COVID-19 rapid serological point-of-care test will be used to identify potential plasma donors.
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Vapotherm’s Oxygen Assist Module wins FDA breakthrough device nod

April 9, 2020
By Meg Bryant
The U.S. FDA has granted breakthrough device designation to Vapotherm Inc. for its Oxygen Assist Module (OAM), for use with its Precision Flow assistive breathing systems. The new module is designed to aid clinicians in maintaining a targeted blood oxygen range in patients requiring oxygen therapy.
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