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BioWorld - Thursday, February 19, 2026
Home » Topics » Regulatory

Regulatory
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Regulatory front for June 25, 2020

June 25, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Alcon, Novartis, Regeneron, Roche.
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Regulatory actions for June 25, 2020

June 25, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: EMD Serono, Genprex, Medivir, Merck, Sinovac, Tizona, Viracta.
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FDA approves Keytruda for recurrent or metastatic cutaneous squamous cell carcinoma

June 25, 2020

Regulatory front for June 24, 2020

June 24, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Advamed, Kbmo Diagnostics.
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Regulatory actions for June 24, 2020

June 24, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Gencurix.
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Regulatory actions for June 24, 2020

June 24, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Fulcrum, GBT, Hemoshear, Imara, Innate, Mayne, Medigene, Neurorx, Novartis, Relief, Philogen.
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Regulatory front for June 24, 2020

June 24, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Gilead, Kymab, Regeneron.
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India-pill-bottle-drugs

India’s Glenmark Pharmaceuticals gets green light to launch $1 COVID-19 treatment tablets

June 23, 2020
By David Ho
HONG KONG - Mumbai-based Glenmark Pharmaceuticals Ltd. has been granted manufacturing and marketing approval for the launch of its antiviral drug, favipiravir, for the treatment of mild to moderate COVID-19, a move it deems a “landmark development for COVID-19 patients in India.”
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Architectural pillars

Regulatory front for June 23, 2020

June 23, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Auromedics, Bring Entrepreneurial Advancements to Consumers Here In North America, Central Drugs Standard Control Organisation, FDA, Gilead Sciences, Medicines and Healthcare products Regulatory Agency, NIH, Pharmaceutical and Medical Devices Agency, Somerset, Therapeutic Goods Administration, U.S. Patent and Trademark Office.
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Man clutching heart

FDA grants breakthrough designation to Precardia’s ADHF system

June 23, 2020
By Liz Hollis
Precardia Inc. received some good news from the U.S. FDA, which has granted the company's catheter-based system for treating volume overload in patients with acutely decompensated heart failure (ADHF) breakthrough device designation. The device is intended to quickly reduce congestion in the venous system, known as cardiac preload, with an eye toward improving overall cardio-renal function.
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