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BioWorld - Tuesday, April 14, 2026
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Regulatory
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Regulatory actions for May 29, 2020

May 29, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Baibies, Letsgetchecked.
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Researcher in PPE looking at three vials

WHO launches COVID-19 patent pool, backed by 35+ countries

May 29, 2020
By Nuala Moran
LONDON – The World Health Organization (WHO) is stepping up its effort to try and ensure equitable access to any approved COVID-19 vaccines and therapies, putting in place a system for sharing all intellectual property, information and clinical trials data needed to enable generic manufacturing.
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Imminent Ebola vaccine approval in Europe a historic first for J&J’s Advac platform

May 29, 2020
By Cormac Sheridan
DUBLIN – Johnson & Johnson’s Janssen Biotech arm is on the brink of a historic first vaccine approval, having secured a positive vote May 29 from the EMA’s Committee for Medicinal Products for Human Use (CHMP) for its prime-boost Ebola virus vaccine combo, Zabdeno (Ad26.Zebov) plus MVABEA (MVA-BN-Filo).
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Regulatory actions for May 29, 2020

May 29, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astellas, Boehringer, Chi-Med, Immune-Onc, J&J, Lilly, Menlo, Nabriva, Novartis, Onxeo, Orphazyme, Roche, Santhera, Takeda.
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Regulatory actions for May 28, 2020

May 28, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Airos Medical, GE Healthcare, Gynesonics, Quest Diagnostics.
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Regulatory front for May 28, 2020

May 28, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Clew Medical, Medtronic.
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Regulatory front for May 28, 2020

May 28, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for May 28, 2020

May 28, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Ashvattha, Basilea, Bird Rock, Cardiff, Cerecor, Chiesi, Immodulon, Macrogenics, Moleculin, Orpheris, Phasebio, Protalix, Roche, Theraly.
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U.S. FDA encouraging COVID-19 test developers to file 510(k)s

May 27, 2020
By Mark McCarty
The number of tests of various types for the SARS-CoV-2 virus are still growing, but the emergency use authorization (EUA) program is not the only option for developers. Timothy Stenzel, director of the Office of In Vitro Diagnostics and Radiology, said on the agency’s May 27 town hall that the agency would like to see test developers file for a 510(k) for their tests when the data are sufficient to support an application, adding that any such clearances will not affect the U.S. FDA’s interest in keeping plenty of similar tests on the market via the EUA mechanism.
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Regulatory front for May 27, 2020

May 27, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Nantong Egens Biotechnology, Ntbio Diagnostics.
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