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BioWorld - Tuesday, December 16, 2025
Home » Topics » Regulatory

Regulatory
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Regulatory actions for May 15, 2020

May 15, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Algernon, Blueprint, BMS, Can-Fite, Clovis, Deciphera, Kancera, Leading Biosciences, Neuraptive, Seelos.
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Lyfaquin approved in India for hypovolemic shock

May 15, 2020

Regulatory front for May 14, 2020

May 14, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Wilmington Island Medical.
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Regulatory actions for May 14, 2020

May 14, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Applied DNA, Medalliance.
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Regulatory actions for May 14, 2020

May 14, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abivax, Aim Immunotech, Cellphire, Enzychem, Immunic, Nordic Nanovector, Pharmazz, Restem, Sanofi, Scimount, Seattle Genetics, Takeda, Verona, Zealand.
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Regulatory front for May 14, 2020

May 14, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Coronavirus vs U.S. wrecking balls

FDA sees swabs as ‘hot topic,’ will hold town hall for 3D-printed swabs

May 13, 2020
By Mark McCarty
The FDA’s weekly town hall on testing for the COVID-19 pandemic included the usual range of concerns about test performance, but concerns regarding swabs and sample sites continue to mount. The predicament has led to the announcement that the FDA along with the National Institutes of Health (NIH) will hold a May 15 town hall regarding swabs, with a particular interest in swabs produced via additive manufacturing.
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Eko device and software in use during in-clinic screening

Eko scores EUA for algorithm to identify heart failure in COVID-19 patients

May 13, 2020
By Meg Bryant
The U.S. FDA has given the greenlight to Eko Devices Inc.’s electrocardiogram (ECG)-based algorithm to aid in detecting patients with heart failure during the COVID-19 pandemic. The artificial intelligence (AI)-powered algorithm, which provides a quick way to screen for low ejection fraction, won FDA breakthrough status in December of 2019.
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Regulatory front for May 13, 2020

May 13, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including the American Clinical Laboratory Association.
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Regulatory actions for May 13, 2020

May 13, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Critical Alert, Eko, Novocure, Optina Diagnostics, Zai Lab.
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