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BioWorld - Sunday, February 15, 2026
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Regulatory front for Feb. 4, 2020

Feb. 4, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: U.S. Department of Justice
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FDA approves Audenz to protect against influenza A (H5N1)

Feb. 4, 2020

Regulatory front for Feb. 3, 2020

Feb. 3, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Johnson & Johnson.
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Influenza A protection and a peanut allergy treatment receive FDA approvals

Feb. 3, 2020
By Lee Landenberger
The FDA has issued two new approvals, one for a cell-based pandemic influenza A (H5N1) vaccine and the other is the first approval for treating peanut allergy.
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Australia’s Mesoblast submits final module of rolling BLA submission for pediatric GVHD stem cell therapy

Feb. 3, 2020
By Tamra Sami
PERTH, Australia – Australian stem cell therapy company Mesoblast Ltd. has filed the final module of its rolling BLA submission for its allogeneic mesenchymal precursor cell therapy, remestemcel-L, after it showed strong survival rates in children with acute steroid-refractory graft-vs.-host disease (aGVHD).
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Japan’s drug repricing plan to hit some top sellers

Feb. 3, 2020
By Jihyun Kim
HONG KONG – Aiming to increase the financial stability of the national health care insurance system, Japan has announced a list of 17 drugs for which prices will be reduced.
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Regulatory front for Feb. 3, 2020

Feb. 3, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Vanda Pharmaceuticals.
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FDA approves Palforzia oral immunotherapy for peanut allergy

Feb. 3, 2020
Brexit hourglass illustration

Brexit day arrives; industry continues to face lack of clarity as transition period begins

Jan. 31, 2020
By Nuala Moran
LONDON – Brexit finally becomes a reality at midnight central European time on Jan. 31, but for the life sciences industry uncertainty continues, as the U.K. enters an 11-month transition phase during which the terms of its future relationship with the EU must be negotiated.
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1-31-Medtronic-Cobalt-XT.png

Medtronic scores CE marking for Bluesync-enabled implantable defibrillators

Jan. 31, 2020
By Meg Bryant
Medtronic plc has gained CE mark approval for its Cobalt and Crome portfolio, the company’s first implantable cardiac defibrillators (ICDs) and cardiac resynchronization therapy-defibrillators (CRT-Ds) to offer connected health via Bluesync technology. The portfolio will be rolled out on a country-by-country basis throughout Europe, with initial implants in select countries to begin soon.
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