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BioWorld - Tuesday, January 6, 2026
Home » Topics » Regions » Asia-Pacific

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Control Bionics raises AU$15M in IPO to fund global expansion

Dec. 11, 2020
By Tamra Sami
PERTH, Australia – Med-tech company Control Bionics began trading on the Australian Securities Exchange (ASX:CBL) Dec. 7 in an IPO that saw the company raise AU$15 million (US$11.25 million). Melbourne-headquartered Control Bionics develops assistive technologies (AT) that allow people with severe disabilities to communicate and control electronic devices using electromyography (EMG).
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Gold chain link engraved with "partnership"

Phar-East 2020 conference brings value and challenges of partnerships into focus

Dec. 10, 2020
By David Ho
HONG KONG – Partnerships are reshaping the pharmaceutical industry across Asia, said speakers during day two of the Phar-East 2020 virtual conference. While industry has “tended to have a go-at-it-alone approach,” doing all its discovery, development and commercialization work in-house, “nothing ever came in or out. I think that’s really changed in recent years,” said Kazia Therapeutics Ltd. CEO James Garner.
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Map, flag of India

Indian rules pave way for mandatory registration, but patent concerns remain

Dec. 9, 2020
By T.V. Padma
NEW DELHI – Recent changes to India’s rules on medical devices have evoked mixed reaction among industry and legal experts with concerns over their impact on patenting of innovations tinged with a welcome reception of a new clause for mandatory registration and licensing of medical devices in the country to improve adherence to quality requirements. 
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Head filled with digital data

Phar-East 2020 virtual conference looks at tech and transformation

Dec. 9, 2020
By David Ho
HONG KONG – New approaches to trials, digitalization and the effective use of advance technologies like artificial intelligence are reshaping how clinical trials are conducted, drugs are discovered, and new devices are developed, said participants at the Asia-focused Phar-East 2020 conference on Dec. 8.
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Pharmaengine inks partnership with Sentinel Oncology for checkpoint kinase 1 inhibitor SOL-578

Dec. 9, 2020
By Gina Lee
HONG KONG – Taipei, Taiwan-based Pharmaengine Inc. has signed a collaboration and licensing deal with Cambridge, U.K.-based Sentinel Oncology Ltd. for the latter’s checkpoint kinase 1 inhibitor, SOL-578. Through the agreement, Sentinel will receive an exclusivity payment and Pharmaengine will fund the IND-enabling studies.
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Dong-ki Lee, CEO, Olix

Olix nabs $38M for core pipeline and RNA synthesis GMP facility

Dec. 8, 2020
By Gina Lee
HONG KONG – Olix Pharmaceuticals Inc. has raised ₩41.5 billion (US$37.90 million) to support the company’s U.S. expansion and advance its pipeline globally.
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Australian flag marking country on globe

Implantable device manufacturers must include patient implant cards, leaflets in Australia

Dec. 4, 2020
By Tamra Sami
PERTH, Australia – Australia's Therapeutic Goods Administration (TGA) is requiring manufacturers of permanently implantable devices to provide patient implant cards and consumer device leaflets with their devices, beginning Dec. 1. New implantable devices will need to comply by Dec. 1, 2020, and existing implantable devices will have until Dec. 1, 2021, to comply.
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Blood cells and bacteria

Antimicrobial polymers AMP up fight against MDR bacteria

Dec. 4, 2020
By John Fox
An international study led by Nanyang Technological University in Singapore has designed and synthesized broad-spectrum antimicrobial polymers (AMPs) and demonstrated the safety and efficacy of two such agents against multidrug-resistant (MDR) bacteria in mouse models of sepsis.
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Dong-ki Lee, CEO, Olix

Olix nabs $38M for core pipeline and RNA synthesis GMP facility

Dec. 4, 2020
By Gina Lee
HONG KONG – Olix Pharmaceuticals Inc. has raised ₩41.5 billion (US$37.90 million) to support the company’s U.S. expansion and advance its pipeline globally.
Read More
Australia map, flag

Australia unveils new framework for personalized medical devices, 3D-printed devices

Dec. 2, 2020
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Good Administration (TGA) has unveiled its final regulatory requirements for personalized medical devices, including 3D-printed devices, that go into effect on Feb. 25, 2021. Under the previous framework, custom-made medical devices were exempt from the requirement to be included in the Australian Register of Therapeutic Goods (ARTG).
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