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BioWorld - Wednesday, June 10, 2026
Home » Topics » Infection » Coronavirus

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Regulatory front for July 20, 2020

July 20, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA, Wright Medical Group.
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BioWorld MedTech’s Cardiology Extra for July 20, 2020

July 20, 2020
By Liz Hollis
Keeping you up to date on recent developments in cardiology, including: COVID-19's influence on broken heart syndrome; Researchers see hope with blood test for advancing heart failure treatment; Antiplatelet med could treat heart attack.
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Regulatory actions for July 20, 2020

July 20, 2020

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Generex, Immuron, Karyopharm, Molecular Partners, Neoimmunetech, Orchard, Orphazyme, Osmotica, Sanifit, Sorrento.


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Other news to note for July 20, 2020

July 20, 2020

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Albireo, Alexion, Can-Fite, Contrafect, Cytocom, Enlivex, Epsilogen, Geneuro, Imquest, Innovation, Inozyme, JW Therapeutics, Kedrion, Mateon, Metaclipse, PTC Therapeutics, Santhera, Sonnet, Vaxil.


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In the clinic for July 20, 2020

July 20, 2020

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Abbvie, Amplyx, Arcutis, Ascletis, Astrazeneca, Basilea, Bergenbio, Bioniz, Biontech, Bioxcel, Connect, Exelixis, Lantern, Pfizer, Synairgen, Vertex.


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Beyond antibodies: T cells are a critical aspect of long-term COVID-19 immunity

July 19, 2020
By Nuala Moran
LONDON – From the start of the pandemic antibodies have been the main focus of attempts to understand the immune response to SARS-CoV-2 and ascertain what it will take for vaccines to be protective.
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Digital illustration of U.S., coronavirus

Trautman: COVID-19 may hamper FDA’s efforts to further harmonize Part 820, ISO 13485

July 17, 2020
By Mark McCarty
The U.S. FDA’s interest in harmonizing its regulations for medical devices with an international standard is a matter of record, but the agency has found this to be an enormously complicated task. Kim Trautman, executive vice president for medical device services at NSF International, of Ann Arbor, Mich., told BioWorld that the task of rewriting Part 820 to meet ISO 13485 in the middle is no mean feat, but also that it may be delayed again, this time because of the COVID-19 pandemic.
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BioWorld MedTech’s Neurology Extra for July 17, 2020

July 17, 2020
By Andrea Applegate
Keeping you up to date on recent developments in neurology, including: Phantom-limb pain reduced through brain-computer interface training; Anxiety, depression in COVID-19 patients with loss of smell and taste; HBOT improves cognitive function of older adults.
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Brexit hourglass illustration

Brexit countdown looming, despite COVID-19 distractions

July 17, 2020
By Nuala Moran
LONDON – While the pandemic raged, Brexit was simmering on the back burner, but now as infections wane, the industry is turning its attention back to being ready for the U.K. cutting ties with the EU at the end of December.
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Other news to note for July 17, 2020

July 17, 2020

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Applied DNA, Aptorum, Bio-Thera, Curadigm, Cyclerion, Fairhaven, Liminal, Ocular, Orphazyme, Pharmapark, Takis.


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