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BioWorld - Monday, February 16, 2026
Home » Topics » Coronavirus, Medical technology

Coronavirus, Medical technology
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Regulatory actions for Dec. 28, 2020

Dec. 28, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Mologic.
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Other news to note for Dec. 28, 2020

Dec. 28, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Amoy Diagnostics, Aytu Bioscience, Concord Healthcare Singapore, Corning, Eurofins Genomics, Merck KGaA, Olympus Partners, Soterix Medical, Titan Medical.
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BioWorld MedTech’s Cardiology Extra for Dec. 28, 2020

Dec. 28, 2020
By Liz Hollis
Keeping you up to date on recent developments in cardiology, including: Differences seen between the sexes in terms of stroke survival; Light used to control cardiac waves; 3D-printed blood vessels ID possible link between coronavirus, stroke.
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Regulatory actions for Dec. 23, 2020

Dec. 23, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Agilent, Carmat, Interscope, Quidel.
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Other news to note for Dec. 23, 2020

Dec. 23, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: 3B Blackbio Biotech, Arbor Biotechnologies, Astrazeneca, Biodesix, Celcuity, Deerfield Management, Eurofins, Excalibur Healthcare Services, Genophyll Enterprises, Identitysensors Biologics, Iridex, Ixlayer, Lgc Maine Standards, Lonza, Mogene, Nanotronics Health, Natural Wellness Clinics, Orasure, Palantir Technologies, Puma Biotechnology, Pwnhealth, Roche, Solutions in Critical Care, Sorrento Therapeutics, Todos Medical, Natural Wellness Clinics.
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U.S. Capitol building

Walden looks at the challenges ahead, milestones behind

Dec. 23, 2020
By Mari Serebrov
In an exclusive interview with BioWorld on the challenges facing a deeply divided Congress and some of the highlights of his years in the U.S. House, retiring Congressman Greg Walden (R-Ore.) said that once the COVID- 19 pandemic is over, federal policymakers should hold a summit with officials from states and major cities to look at a new preparedness partnership that would ensure the availability of strategic medical supplies.
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Product image

Dymedso’s Frequencer clears the air in severe COVID-19 cases

Dec. 22, 2020
By David Godkin
TORONTO – An airway clearance device that uses acoustic sound waves to treat lung disorders and respiratory infections like cystic fibrosis (CF) is now being used to clear the lungs of patients suffering very badly from COVID-19. Developed by Montreal-based Dymedso Inc., more than 675 Frequencer acoustic devices currently being utilized across the world are assisting COVID-19 patients by removing mucous and secretions from their lungs and smaller airways.
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Other news to note for Dec. 22, 2020

Dec. 22, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Biolog-id, Biomérieux, Biointellisense, Brattle Street Investment, Change Healthcare, Cobham Advanced Electronic Solutions, Co-Diagnostics, Compugroup Medical, Dariohealth, Electrocore, Emd, Grove Biomedical, Hancock Jaffe Laboratories, Heru, Honeywell, Hyro, Intel, Nexus Dx, Osang Healthcare, Philips, Pro Medical Baltic, Purlab, Quest Diagnostics, Salona Global Medical Device, Siemens Healthineers, Spineway, Traction Guest, Twist Bioscience, Teladoc, World Telehealth Initiative, Zuora.
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Regulatory actions for Dec. 22, 2020

Dec. 22, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acell, Artms, Medtronic, Products + Features, Quidel, Rapid Medical.
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European Union map and coronavirus

EMA authorizes Pfizer/Biontech vaccine as new SARS-CoV-2 variant emerges

Dec. 21, 2020
By Nuala Moran
LONDON – The EMA has issued a positive opinion on Pfizer Inc./Biontech SE’s COVID-19 vaccine, BNT-162b2, becoming the first regulator to recommend a full marketing authorization, rather than approval for emergency use. The vaccine, now brand named Comirnaty, still has to go through the formality of being approved by EU member state governments, but the EU health commissioner, Stella Kyriakides, has said she expects roll out to start on Dec. 27.
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