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BioWorld - Friday, July 17, 2026
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Regulatory
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Regulatory actions for March 4, 2021

March 4, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Kronos, Nervgen, Nicox, Novadip, Ocumension, Pfizer, RDIF, Regeneron, Sanofi.
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Device image

Front Line’s small aortic occlusion device approved in Canada

March 3, 2021
By David Godkin
TORONTO – Front Line Medical Technologies Inc. reported Health Canada approval for a device deemed the smallest for use in emergency situations when patients require hemodynamic support to maintain blood flow to the brain and heart. According to biomedical engineer, co-founder and Front Line CEO Asha Parekh, the Cobra-OS is the world’s smallest REBOA (Resuscitative Endovascular Balloon Occlusion of the Aorta) device.
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Regulatory front for March 3, 2021

March 3, 2021
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: GAO reviews FEMA's pandemic supply chain management efforts; Testing lab owner sentenced to three years; Health Canada renews interim order for importation of devices; FDA: claims of registration certificates may be misleading; MDCG issues gap guidance pending Eudamed completion; FDA seeking nominations for advisory committee.
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Regulatory actions for March 3, 2021

March 3, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Asensus Surgical, Medalliance.
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WTO head: Vaccine companies must license sites in emerging countries

March 3, 2021
By Mari Serebrov
As the World Trade Organization (WTO) debate intensified this week over a demand to waive patent protections for COVID-19 vaccines and therapies, the group’s new director-general, Ngozi Okonjo-Iweala, urged members to “walk and chew gum” at the same time by working with “companies to open up and license more viable manufacturing sites now in emerging markets and developing countries. We must get them to work with us on know-how and technology transfer now.”
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Regulatory front for March 3, 2021

March 3, 2021
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for March 3, 2021

March 3, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Blueprint, Dialectic, Exicure, Exithera, Idorsia, Junshi, Kempharm, Oblato, On Target, RDIF, Saniona, Sorrento, Wellmarker, Xentria.
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ADHD carved into desktop

FDA approves new once-daily ADHD drug Azstarys

March 3, 2021
By Michael Fitzhugh
A new once-daily attention deficit hyperactive disorder (ADHD) drug developed by prodrug specialist Kempharm Inc. has won FDA approval under the brand name Azstarys. The medicine combines serdexmethylphenidate, Kempharm's prodrug of the CNS stimulant dexmethylphenidate, with immediate-release d-MPH, the core medicine in the now off-patent product Focalin, a refined formulation of Ritalin.
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FDA approves Azstarys for ADHD

March 3, 2021
COVID-19 vaccine vials

Two COVID-19 vaccines approved in China in less than 24 hours

March 2, 2021
By Sergio Held
China’s National Medical Products Administration granted conditional approval two Chinese-developed COVID-19 vaccines in less than 24 hours on Feb. 25. One of the vaccines approved was developed by Tianjin-based Cansino Biologics Inc., and the other by China National Pharmaceutical Group (Sinopharm) through its Wuhan Institute of Biological Products subsidiary.
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