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BioWorld - Saturday, July 11, 2026
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Regulatory actions for June 4, 2020

June 4, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Bausch + Lomb, Roche, Synedgen, Transit Scientific.
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Map of Europe

Update to ISO 14155 delayed, alignment with EU MDR remains uncertain

June 4, 2020
By Mark McCarty
The implementation date for the EU’s new med-tech regulatory framework has been pushed back a year, giving device makers much-needed breathing room for compliance work. At the same time, the International Organization for Standardization (ISO) has not fulfilled the planned May update of its device clinical investigations standard, ISO 14155.
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Beigene’s FDA-cleared BTK inhibitor Brukinsa approved in China

June 4, 2020
By Elise Mak
Chinese biotech firm Beigene Ltd. said its second-generation BTK inhibitor, Brukinsa (zanubrutinib), has won approval in China for two indications, entering a market dominated by Imbruvica (ibrutinib, Johnson & Johnson/Abbvie Inc.). The NDA approval came eight months after Brukinsa’s clearance in the U.S.
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Regulatory front for June 4, 2020

June 4, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Almirall, Amneal.
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Regulatory actions for June 4, 2020

June 4, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aldeyra, Algernon, Anavex, Can-Fite, Elixirgen.
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Brukinsa receives approval in China for patients with CLL/SLL and MCL

June 4, 2020

FDA’s Stenzel says standards for molecular tests for SARS-CoV-2 a good approximation for NGS testing

June 3, 2020
By Mark McCarty
The latest U.S. FDA town hall for testing for the COVID-19 included a few updates on serological testing, but perhaps the most important take-away was when Tim Stenzel, director of the Office of In Vitro Diagnostics and Radiology, advised attendees that performance expectations regarding next-generation sequence (NGS) testing for the SARS-CoV-2 virus will closely resemble those of conventional molecular testing.
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Cpass test kit components

Genscript seeks EUA for test that indicates immunity to COVID-19

June 3, 2020
By Meg Bryant
As more COVID-19 antibody testing becomes available, one question has been on everybody’s mind: Does the presence of antibodies to SARS-CoV-2, the virus responsible for the global pandemic, mean that people are protected from future infection? To that end, Genscript Biotech Corp., of Piscataway, N.J., has applied for emergency use authorization (EUA) with the U.S. FDA to market a test that specifically recognizes neutralizing antibodies to SARS-CoV-2.
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Regulatory front for June 3, 2020

June 3, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies.
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Regulatory actions for June 3, 2020

June 3, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Axonics, Fractyl, Surgical Information Sciences.
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