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

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BioWorld MedTech’s Diagnostics Extra for July 9, 2020

July 9, 2020
By Meg Bryant and Anette Breindl
Keeping you up to date on recent developments in diagnostics, including: Diagnosing fatty liver disease; Assessing COVID-19 with lung ultrasound; Noncoding mutations contribute to heart disease.
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Mylan gets remdesivir approval for COVID-19 in India

July 9, 2020
By David Ho
HONG KONG – The Drug Controller General of India (DCGI) has approved Mylan NV’s remdesivir 100-mg vial for restricted emergency use in COVID-19 cases.
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Regulatory actions for July 9, 2020

July 9, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Allergy, Anaptysbio, Assembly, Astrazeneca, Chemocentryx, Crinetics, Fate, Fujifilm, Immodulon, Leo, Merck, Mylan, Osmotica.
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Other news to note for July 9, 2020

July 9, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: AGC, Aim Immunotech, Alimera, Altimmune, Anergis, Ardigen, Astrazeneca, BC Neuroimmunology, Bioxcel, Chromadex, CVC, Cytodyn, Dynport, Hemoshear, Hypertrust, Ilya, Innocan, Kaléo, Kronos, Kye, Moderna, Molecular Partners, Molmed, Novelion, Optinose, Orchard, Promis, Proteinqure, Recipharm, Renovion, Stoke, Therapix, Transgene, Tris, Virometix.
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Osivax secures $36M in grant, equity funding for flu, coronavirus vaccine programs

July 8, 2020
By Cormac Sheridan
DUBLIN – Osivax SAS has assembled a public funding package of more than €32 million (US$36.3 million) to pursue ongoing clinical development of its universal flu vaccine and to take forward a coronavirus vaccine program based on a similar approach, involving vaccine-like particle (VLP) technology.
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Product image

Nonin nabs FDA nod for wireless handheld for first responders to monitor oxygen indicators

July 8, 2020
By Stacy Lawrence
Plymouth, Minn.-based Nonin Medical Inc. gained a U.S. FDA 510(k) clearance for its Co-Pilot wireless hand-held multiparameter system (H500). The system is expected to be used by first responders to evaluate various oxygenation and respiratory-related parameters in patients after incidents such as cardiac arrest, traumatic injury, carbon monoxide or smoke inhalation.
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Patient given oral swab

U.S. FDA urges test developers to amend EUAs for pooled sample testing

July 8, 2020
By Mark McCarty
The U.S. FDA’s priorities for testing for the SARS-CoV-2 virus have shifted as circumstances have changed, and the agency is putting more emphasis into testing of pooled samples. Toby Lowe, the associate director of the Office of In Vitro Diagnostics and Radiological Health (OIR), said on the July 8 diagnostic town hall that the agency wants to encourage test developers to work on their existing EUAs for pooled sampling.
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Patient video chatting with doctor on mobile phone

Doctor On Demand raises $75M in series D

July 8, 2020
By Meg Bryant
Virtual care provider Doctor On Demand has scooped up $75 million in a series D round led by General Atlantic, with participation from existing investors. The funds are earmarked to fuel the company’s growth and expand access to comprehensive telehealth services across the U.S. Combined with earlier financings, the San Francisco-based company has raised nearly $240 million to date.
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Regulatory front for July 8, 2020

July 8, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Luminex, Modern Allergy Management, WHO.
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Regulatory actions for July 8, 2020

July 8, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Balt, Nonin Medical, Saladax Biomedical, Urocam.
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