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BioWorld - Monday, July 20, 2026
Home » Topics » Infection » Coronavirus

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FDA says new lab test combination possible if existing assay EUA is updated for new instrument

Nov. 4, 2020
By Mark McCarty
The U.S. FDA’s stated policy is that it will not review emergency use authorizations (EUAs) for lab-developed tests (LDTs) for the COVID-19 pandemic, but that doesn’t mean labs are completely shut out. The FDA’s Toby Lowe said that a lab that wants to pair an assay that already has an EUA with a new software installation on lab instrumentation can work with the assay developer to update that EUA.
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Other news to note for Nov. 4, 2020

Nov. 4, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Applied UV, Axsome Therapeutics, Clinical Laserthermia Systems, Digirad, Electromedical Technologies, Energetic Wellness School of Naturopathy, The Feinstein Institutes for Medical Research, Mimedx, Novan, Ontrak, Stryker, Thermo Fisher Scientific, Toyoda Gosei, Wright Medical Group.
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In the clinic for Nov. 4, 2020

Nov. 4, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Mauna Kea Technologies, Truvian.
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BioWorld MedTech’s Orthopedics Extra for Nov. 4, 2020

Nov. 4, 2020
By Holland Johnson
Keeping you up to date on recent developments in orthopedics, including: New opportunities for detecting osteoporosis; Brazilian researchers discover how muscle regenerates after exercise; Different outcomes by race/ethnicity among patients with COVID-19 and rheumatic disease.
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Humanigen makes first foray in Asia Pacific with deal for COVID-19 treatment

Nov. 4, 2020
By David Ho
HONG KONG – Humanigen Inc. has executed its first licensing agreement in the Asia-Pacific region, in a deal worth up to $20 million that gives Telcon RF Pharmaceutical Inc. and KPM Tech Co. Ltd. the development and commercialization rights to lenzilumab for COVID-19 in South Korea and the Philippines.
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Other news to note for Nov. 4, 2020

Nov. 4, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Axsome, Bristol, Equillium, Generex, Ionis, Jubilant, Myokardia, Novan, Novavax, Ocular, Pfizer, Prothena, Salliant, Sofie.
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Regulatory front

FDA issues advisory regarding false positive antigen tests

Nov. 3, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA announces recall of discontinued Medtronic catheter.
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Regulatory actions for Nov. 3, 2020

Nov. 3, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbott, Biolytical Laboratories, DNA Genotek, Pari Pharma, Salvia Bioelectronics.
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Other news to note for Nov. 3, 2020

Nov. 3, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alveo Technologies, Biocartis Group, Coloplast, Decision Diagnostics, DJO Global, Endpoint Health, Geneprodx, Hutchinson Technology, Joline, Mir Scientific, Morton Comprehensive Health Services, Motus GI, Nine Continents Medical, Novarad, Ossdsign, Oxford Gene Technology, Remark Holdings, Resonetics, Sirakoss, Stryker, Wright Medical Group.
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Other news to note for Nov. 3, 2020

Nov. 3, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Bioasis, Calliditas, CEPI, Checkpoint, Clover, Genkyotex, Hoth, Humanigen, Immunoprecise, Inventiva, KPM, Minoryx, Sichuan Clover, Telcon RF, TLC, Xoma.
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