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Home » SARS-CoV-2

Articles Tagged with ''SARS-CoV-2''

Other news to note for Sept. 9, 2020

Sep. 9, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Ambu, Analog Devices, A.R.C. Laser, Avricore Health, Benchmark Electronics, Change Healthcare, Clearside Biomedical, Coracoid Solutions, Coremap, D&D Pharmatech, Dnanudge, Evonetix, Fotona, Genova Diagnostics, Gogomeds, Hospitec, Joint Commission, Kit Check, Lifelabs, Livongo, Lncbio, Magellan Health, Medline Industries, Nanostring, Nanox, Orexo, Paradise Genomics, Parvizi Surgical Innovation, Personal Genome Diagnostics, Pharmigene, Regenexbio, Respiration, Rocky Mountain Analytical, S2 Genomics, Sca Pharma, Scrum, Spi Medical, Sqi Diagnostics, Thermo Fisher Scientific, Thrive Health, Thunderbio Science, Trendbio, Vizient.
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In the clinic for Sept. 9, 2020

Sep. 9, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Alydia Health, BD, Dreamed Diabetes, Sight Sciences.
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Coronavirus vaccine illustration

Spybiotech, Serum Institute of India partner on VLP-based COVID-19 vaccine

Sep. 8, 2020
By Cormac Sheridan
DUBLIN – Spybiotech Ltd. has secured a first vaccine deal for its proprietary Spytag/Spycatcher protein conjugation technology. The Serum Institute of India Pvt. Co. Ltd. (SIIPL) is employing the technology in a COVID-19 virus-like-particle (VLP)-based vaccine, which recently entered a phase I/II trial in Australia. An initial data readout is expected in October or November.
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Other news to note for Sept. 8, 2020

Sep. 8, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Acutus, Alkahest, Arches Research, Assure Holdings, Avacta, Cambus Medical, Co-Diagnostics, Confirm Biosciences, Cytosorbents, Diagnos, Diasorin, Fluidigm, Freudenberg Medical, Grifols, Inovio, Irhythm, Labcorp, Memed, Merit Medical, Neuronostics, Polarity TE, Qiagen, Roche Canada, Seegene, Thermo Fisher Scientific.
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Regulatory actions for Sept. 4, 2020

Sep. 4, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Roche.
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In the clinic for Sept. 4, 2020

Sep. 4, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Gelesis, Medmira.
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Mobiledetect Bio BCC19 test kit

Detectachem wins EUA for rapid COVID-19 test kit

Sep. 3, 2020
By Mary Ellen Schneider
Detectachem Inc. has scored an emergency use authorization (EUA) from the U.S. FDA to market a new molecular RNA test kit for SARS-CoV-2 that provides color-coded results in about 30 minutes.
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Plasma bag

Dueling plasma guidelines a sign of the times

Sep. 3, 2020
By Mari Serebrov
While the emergency use authorization (EUA) the FDA granted Aug. 23 for convalescent plasma remains a political talking point, the agency moved ahead Sept. 2, issuing an updated, immediately effective guidance on the use of convalescent plasma to treat COVID-19 patients in ongoing clinical trials, on an expanded access basis or under the EUA.
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Other news to note for Sept. 3, 2020

Sep. 3, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Abbott, Acarix, Access Biologicals, Aditx Therapeutics, Caredfor, Castlight Health, Centogene, Deep Longevity, Fivebase, Fulgent Genetics, Gateway Foundation, Guardian Research Network, Henry Schein, Impulse Dynamics, Indemic, Intermountain Healthcare, Lumithera, MDclone, Mcmaster Healthlabs, Oncocyte, Regent Pacific, Safeology, Speedx, Verto Health, Viz.ai, Salveo Diagnostics, Zyris.
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Disintegrating coronavirus

Roche to unveil rapid antigen test for COVID-19

Sep. 2, 2020
By Liz Hollis
As the COVID-19 pandemic continues into the fall, Roche Group is planning to launch its latest tool later this month. And while its SARS-CoV-2 Rapid Antigen Test will be available in markets accepting the CE mark, the company is expecting the filing for emergency use authorization (EUA) from the U.S. FDA. Roche’s test is a rapid chromatographic immunoassay intended for the qualitative detection of a specific antigen of SARS-CoV-2 present in human nasopharynx.
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