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BioWorld - Wednesday, February 11, 2026
Home » Topics » Regulatory

Regulatory
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Regulatory front for Aug. 26, 2020

Aug. 26, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Apotex, Auspex, Glenmark, Johnson & Johnson, Sandoz, Teva, Taro.
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Regulatory actions for Aug. 26, 2020

Aug. 26, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: 3Sbio, Alimera, Hansa, Hifibio, Catalyst, Kye, Revive, TLC.
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Architectural pillars

Regulatory front for Aug. 25, 2020

Aug. 25, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Department of Health and Human Services, Drug Enforcement Administration, FDA, Health Canada, National Center for Advancing Translational Sciences, SK Biopharma.
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Stempeutics’ Stempeucel for critical limb ischemia approved in India

Aug. 25, 2020
By Gina Lee
HONG KONG – Stempeutics Research Pvt Ltd. received the green light from the Drug Controller General of India (DCGI) to launch its Stempeucel therapy to treat critical limb ischemia (CLI) due to Buerger’s disease and atherosclerotic peripheral arterial disease.
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Regulatory front for Aug. 25, 2020

Aug. 25, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: ASP, Genzyme, Smiths Medical, WLF.
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Regulatory actions for Aug. 25, 2020

Aug. 25, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: B. Braun, Gyroscope, Philips, Sientra.
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Rare disease illustration

Ipsen back on track with palovarotene in FOP

Aug. 25, 2020
By Cormac Sheridan
DUBLIN – Ipsen SA is on track for an NDA filing for palovarotene in fibrodysplasia ossificans progressiva (FOP), an ultra-rare disease characterized by the gradual replacement of skeletal muscle and connective tissue with bone, following an interim analysis of phase III data which indicates that the drug may have a substantial effect on the disease process.
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Biopharma opts for collaboration, not patent pools

Aug. 25, 2020
By Mari Serebrov
The idea of patent pools such as the COVID-19 Technology Access Pool (C-TAP) created by the World Health Organization a few months ago has drawn a lot of support from low- and middle-income countries and a handful of wealthier ones, but not so much from industry.
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Bags of plasma

EUA broadens access to plasma in U.S., raises questions about trial enrollment

Aug. 25, 2020
By Mari Serebrov
As of Aug. 13, more than 90,000 patients hospitalized in the U.S. with COVID-19 already had been given access to convalescent plasma through a national expanded use protocol (EAP) sponsored by the Mayo Clinic. The FDA’s decision Sunday to grant emergency use authorization (EUA) for the potential therapy will further expand access to convalescent plasma for hospitalized patients throughout the country at a time when fully approved COVID-19 treatments are nonexistent and even EUAs are few and far between.
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Regulatory front for Aug. 25, 2020

Aug. 25, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Dusa, Wintac.
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