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BioWorld - Friday, February 20, 2026
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4-2-Outset-Medical-tablo.png

FDA greenlights Outset Medical’s Tablo for home dialysis

April 2, 2020
By Meg Bryant
With the COVID-19 pandemic overwhelming hospitals and treatment centers, San Jose, Calif.-based Outset Medical Inc. scored a big win with U.S. FDA clearance of its Tablo hemodialysis system for home dialysis use. The company will begin rolling the system out for home patients in the coming months, balancing that program with demand for onsite devices to support an upswell in COVID-driven dialysis treatments.
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Regulatory front for April 2, 2020

April 2, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Cellex, Ipsum Diagnostics, Refocus Group.
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COVID-19 strikes again: U.S. lawmakers say longer comment periods needed

April 2, 2020
By Mari Serebrov
Given the evolving COVID-19 situation, U.S. House committee chairs are asking the White House Office of Management and Budget (OMB) to direct federal agencies to immediately extend all public comment periods by at least 45 days beyond the end of the declared national emergency, whenever that may be.
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FDA approves Sevenfact for hemophilia A and B

April 2, 2020
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Oncosil wins CE mark, breakthrough designation for pancreatic cancer device

April 1, 2020
By Tamra Sami
PERTH, Australia – The British Standards Institute (BSI) granted Sydney-based Oncosil Medical Ltd. European CE marking approval for its brachytherapy device to treat locally advanced pancreatic cancer in combination with chemotherapy, clearing the way for marketing in both the EU and the U.K. BSI also granted the Oncosil device breakthrough therapy designation.
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ABM-respiratory-biwaze-cough-system.png

FDA nod for ABM Respiratory Care’s Biwaze Cough system

April 1, 2020
By Meg Bryant
Charleston, S.C.-based startup ABM Respiratory Care has received U.S. FDA clearance for its first product, an airway clearance system known as Biwaze Cough. The portable device helps to remove secretions for people who are unable to cough or clear away secretions effectively on their own due to injury or disease.
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Regulatory front for April 1, 2020

April 1, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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Hydroxychloroquine prescription bottle

Desperation drives shortage of antimalarial drugs used to treat COVID-19

April 1, 2020
By Mari Serebrov
The jury is still out on how much hydroxychloroquine and chloroquine actually help in the treatment or prevention of COVID-19, but desperate times have led desperate health care providers to use the antimalarial drugs to treat patients in desperate need of coronavirus cures.
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FDA accepts Mesoblast’s BLA for pediatric GVHD stem cell therapy under priority review

April 1, 2020
By Tamra Sami
PERTH, Australia –Australian stem cell therapy company Mesoblast Ltd. announced that the FDA has accepted its BLA for priority review for its allogeneic mesenchymal precursor cell therapy, remestemcel-L, for children with acute steroid-refractory graft-vs.-host disease (aGVHD).
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Regulatory front for April 1, 2020

April 1, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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