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BioWorld - Tuesday, June 30, 2026
Home » Topics » Regulatory

Regulatory
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Regulatory actions for May 6, 2020

May 6, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Headsafe, Foundation Medicine, Setpoint Medical.
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Astrazeneca's Farxiga wins FDA approval to reduce heart failure risks

May 6, 2020
By Michael Fitzhugh
With new a FDA approval for a years-old type 2 diabetes drug, Astrazeneca plc's Farxiga (dapagliflozin) has become the first sodium-glucose co-transporter 2 (SGLT2) inhibitor to be approved to reduce the risk of cardiovascular (CV) death and hospitalization for heart failure patients with reduced ejection fraction, a measure of how much blood the left ventricle pumps out with each contraction.
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Regulatory front for May 6, 2020

May 6, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Abbvie, Allergan, Astrazeneca, Nestle SA, Sagent Pharmaceuticals, Nichi-Iko Pharmaceutical, WPD Pharmaceuticals, Moleculin Biotech, CNS Pharmaceuticals.
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Regulatory actions for May 6, 2020

May 6, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: AB, Antabio, Astrazeneca, BMS, Cabaletta, Immunicum, Interna, Kiadis, Laurent, Medivir, Pulmotect, Zia.
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FDA approves Farxiga for HFrEF

May 6, 2020
Diagram of SSO2 use for heart

Zoll's Supersaturated Oxygen Therapy receives CE mark

May 5, 2020
By Annette Boyle
Zoll Medical Corp., of Chelmsford, Mass., received CE mark approval to market its second-generation Supersaturated Oxygen (SSO2) Therapy in Europe and other countries that accept CE mark. The therapy, which delivers hyperbaric levels of oxygen to the ischemic heart muscle immediately following percutaneous coronary intervention, has been shown to significantly reduce damage to the heart muscle after an acute myocardial infarction.
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U.S. flag on columned building

2020 Special 301 report calls out the usual U.S. trade partners for IP offenses

May 5, 2020
By Mari Serebrov
Saudi Arabia, which last year made its first appearance on the U.S. Trade Representative’s (USTR) Priority Watch List, is back on the list this year and is being singled out for an out-of-cycle review due to what the USTR calls its “unfair commercial use” and “unauthorized disclosure” of proprietary data submitted for drug approvals.
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Regulatory front for May 5, 2020

May 5, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Chugai, Pfizer, Roche, Therapeutic Goods Administration.
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Regulatory front for May 5, 2020

May 5, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Advamed.
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Regulatory actions for May 5, 2020

May 5, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Bio-Rad, Euroimmun, Lifesignals, Nuvasive, Vitalconnect.
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