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BioWorld - Friday, June 26, 2026
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Home » Topics » BioWorld Asia, Regulatory

BioWorld Asia, Regulatory
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Architectural pillars

Regulatory front for Sept. 8, 2020

Sep. 8, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Amarin, CDC, COVID-19 Treatment Guidelines Panel, Dr. Reddy’s, FDA, Hikma, NIH.
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Skin, tissue layer illustration

After AU$45M IPO, Aroa rakes in two new approvals as it ramps up commercial presence

Sep. 1, 2020
By Tamra Sami
PERTH, Australia – After its initial public offering on the Australian Securities Exchange, soft tissue regeneration company Aroa Biosurgery Ltd. has received new clearances in the U.S. and Europe and is focusing on building up its commercial and manufacturing capacity.
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Architectural pillars

Regulatory front for Sept. 1, 2020

Sep. 1, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Department of Justice, Dusa, FDA, Michbio, Russian Ministry of Health, SEC, Stericycle Expert Solutions, Wintac.
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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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NS Pharma’s Viltepso cleared to take on troubled DMD drug Vyondys

Aug. 18, 2020
By Jennifer Boggs
The FDA granted accelerated approval to Viltepso (viltolarsen) to treat Duchenne muscular dystrophy patients (DMD) who have a confirmed mutation of the DMD gene amenable to exon 53 skipping, pitting it against Sarepta Therapeutics Inc.’s Vyondys (golodirsen), which was given accelerated approval last year in a controversial decision by the FDA following an agency complete response letter (CRL) highlighting safety concerns.
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Architectural pillars

Regulatory front for Aug. 18, 2020

Aug. 18, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Medicines and Healthcare Products Regulatory Agency, Moderna, Office of the U.S. Trade Representative, Pan American Health Organization, SEC, Therapeutic Goods Administration, World Health Organization.
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Amyloid plaque on nerve cell

Yes we aducanumab? Biogen/Eisai AD bid gains traction, outlook still divided

Aug. 11, 2020
By Randy Osborne
News from Biogen Inc. and partner Eisai Co. Ltd. that U.S. regulators accepted the BLA related to aducanumab for Alzheimer’s disease (AD) – and assigned it priority review, no less – set Wall Street abuzz.
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Ascletis’ all-oral HCV treatment approved for marketing in China

Aug. 11, 2020
By Bryan Wong
HONG KONG – The recent approval of all-oral hepatitis C virus (HCV) drug RDV/DNV, a combination of Asclevir (ravidasvir) and Ganovo (danoprevir), helped boost shares of Ascletis Pharma Inc. (HK:1672), which ended July with a 10% jump to HK$3.36 (US43 cents), as the Hangzhou, China-based company continues to push its pipeline of treatments forward and improve its outlook.
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Pakistan flag-map

Import bans hit Pakistan’s pharma industry

Aug. 11, 2020
By Khawar Khan
KARACHI, Pakistan – Geopolitics and a fraught relationship with its neighbors are hurting Pakistan’s pharmaceutical industry and the ability of people to access active pharmaceutical ingredients (APIs) and modern drugs.
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