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BioWorld - Tuesday, January 27, 2026
Home » Topics » Diagnostics, BioWorld MedTech

Diagnostics, BioWorld MedTech
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Lung cancer illustration

Asian precision medicine initiative for lung cancer turns to Thermo Fisher

Sep. 30, 2020
By Annette Boyle
The Lung Cancer Genomic Screening Project for Individualized Medicine in Asia (LC-SCRUM-Asia) has partnered with Thermo Fisher Scientific Inc. to speed molecular profiling in two major studies. The project now uses Waltham, Mass.-based Thermo Fisher’s Ion Torrent Genexus system and Oncomine Precision assay as the sole system for conducting next-generation sequencing (NGS) to improve personalization of therapeutic approaches and better understand drug resistance in non-small-cell lung cancer (NSCLS).
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Product image

Omnivision reveals first medical RGB-IR image sensor

Sep. 30, 2020
By Annette Boyle
Omnivision Technologies Inc. has developed the first all-in-one RGB-infrared image sensor designed for medical use. The OHO2A1S sensor offers simultaneous white-light RGB and infrared monochrome captures in one complementary metal oxide semiconductor sensor, enabling endoscopes used in oncology to be produced with just one sensor, reducing the size, cost and heat output of the devices.
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Micrographic image of coronavirus

Oxford Immunotec teams up with PHE for trial of T-Spot Discovery

Sep. 29, 2020
By Nuala Moran
LONDON – Oxford Immunotec plc is aiming to plug a significant gap in the COVID-19 diagnostics landscape, with the development of a commercial clinical grade test for quantifying T cell responses to the SARS-CoV-2 virus. T-Spot Discovery SARS-CoV-2, currently available for research use only, is based on the same automated technology as the company’s tuberculosis diagnostic, which is approved for use in more than 60 countries.
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Hand holding FDA blocks

Fourth time a charm as FDA finalizes POC blood glucose meter guidance

Sep. 28, 2020
By Mark McCarty
The U.S. FDA’s effort to compile a guidance for prescription, point-of-care (POC) blood glucose meter (BGM) test systems seems to show that guidances can be as iterative as the devices they govern. The FDA announcement for the Sept. 28, 2020, final guidance said that the differences between the 2020 final and the 2018 draft include “a minor edit” regarding user accessibility and a technical correction for hemoglobin testing concentration, yielding a document that is finally ready for prime time after four tries over six years.
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RNA

Blood-based test IDs viral infection before symptoms appear

Sep. 25, 2020
By Meg Bryant
A team of scientists at Duke Health has identified biomarkers that accurately detect viral infections before a person becomes symptomatic. The findings were published in The Lancet Infectious Diseases.
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AI silhouette

Bioplus Interphex Korea: Novartis optimistic about future with AI

Sep. 25, 2020
By Gina Lee
HONG KONG – Novartis AG was cited during the recent 2020 KoNECT-MOHW-MFDS International Conference as an example of a biopharma firm staying ahead of the artificial intelligence curve. During this week’s 2020 Bioplus Interphex Korea conference, Won Kim, head of innovation at Novartis Korea, described some of the firm’s latest forays into AI, including negotiations with potential partners to develop an AI image analysis solution for retinal diseases.
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Product image

Data supports accuracy and performance of Nucleix’s Bladder Epicheck in NMIBC surveillance

Sep. 24, 2020
By Meg Bryant
An independent analysis of studies of Nucleix Ltd.’s Bladder Epicheck demonstrate high diagnostic accuracy and performance in monitoring for disease recurrence in patients with non-muscle invasive bladder cancer (NMIBC).
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Illumet

Australia’s Telix Pharmaceuticals submits NDA for prostate cancer companion diagnostic

Sep. 24, 2020
By Tamra Sami
PERTH, Australia – Melbourne-based Telix Pharmaceuticals Ltd. has submitted its first new drug application to the FDA for TLX591-CDx, a radiopharmaceutical targeting prostate-specific membrane antigen (PSMA) for imaging prostate cancer using positron emission tomography (PET).
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Brain clay model

Cognoa moves ahead on FDA clearance of digital autism diagnostic

Sep. 24, 2020
By Meg Bryant
Children with autism spectrum disorder (ASD) can face a lifetime of frustration because of challenges with communication, social behaviors and flexibility of thought. Early intervention can improve outcomes, but nailing a diagnosis of ASD often takes years. Cognoa Inc. wants to change that with its digital ASD Diagnostic and is on track to apply for U.S. FDA clearance before the end of the year.
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Graph of COVID-19 patient outcome trajectories

Who lives, who dies: Two leading health systems provide mortality calculators for COVID-19

Sep. 23, 2020
By Annette Boyle
Two studies seek to answer the most pressing question for physicians examining a patient with COVID-19: What's this person's risk of death? Mount Sinai researchers presented their clinical prediction model in The Lancet Digital Health and a team from Johns Hopkins published their risk calculator in the Annals of Internal Medicine.
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