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BioWorld - Sunday, July 12, 2026
Home » Topics » Conferences, BioWorld Asia

Conferences, BioWorld Asia
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HKEX exterior

HKEX Biotech Summit 2022 zooms in on biopharma investment trends

Sep. 6, 2022
By Doris Yu
Investments in early stage biotech companies were in focus at the Hong Kong Stock Exchange’s (HKEX) Biotech Summit 2022. The virtual event on Sept. 1 saw discussions centered on this investment trend for younger biotech firms, which looks to be where capital is headed in the sector after a cooldown for listings in Chinese stock markets in the first half of 2022.
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BIO Asia-Taiwan 2022

Taiwan's government embraces biotech startups, but need for capital, greater visibility remain

Aug. 23, 2022
By Tamra Sami
Growing the international competitiveness of Taiwan’s biotech sector is one of six key strategies Taiwan’s government is heavily invested in, Taiwan President Tsai Ing-wen told attendees via video during the recent BIO Asia-Taiwan conference in Taipei.
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Asia at night from space
BIO Asia-Taiwan 2022

Big pharma looks to Taiwan for precision medicine partnerships

Aug. 2, 2022
By Tamra Sami
Big pharma is increasingly turning to Taiwan to leverage the power of the country’s data and computing power as precision medicine takes center stage in drug development, speakers said during the recent BIO Asia-Taiwan conference in Taipei.
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AI silhouette
BIO Asia-Taiwan 2022

Taiwan can help biopharma use data more smartly to keep innovation moving

Aug. 2, 2022
By Tamra Sami
Keeping innovation growing at a fast clip while retaining new global supply chain capacity built up during the pandemic were the main topics of discussion at the Bio Asia-Taiwan conference July 27 in Taipei. With the theme of the conference, “Connecting the Asia Value Chain,” Taiwan Vice President Ching-Te Lai said the pandemic has demonstrated Taiwan’s resilience as well as the strength of the global biopharma industry.
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BIO 2022: Global trials face core challenges from privacy laws

June 28, 2022
By Michael Fitzhugh
As a growing roster of nations moves to protect individual genomic and other health data in the name of privacy under the General Data Protection Regulation in the EU and similar laws elsewhere, chief aggregators of such data, drug developers, are struggling.
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Head filled with digital data

BIO 2022: Push to model disease biology advancing, but slowly

June 21, 2022
By Michael Fitzhugh
With just 10% of therapeutic programs successfully moving from first toxicity dose to market, drug developers are on a constant hunt for new tricks to put the odds in their favor. Strategies abound, from biomarker-guided patient selection to deeper regulatory engagement. But big pharma executives and an academic expert weighing the challenge at the BIO International Convention said June 14 they see another tool slowly gaining traction with the potential to decrease timelines and boost chances for approval: in-silico modeling.
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Conference data for June 14, 2022: ENDO

June 21, 2022
New and updated preclinical and clinical data presented by biopharma firms at the Endocrine Society, including: Astellas, Innovent.
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Conference data for June 14, 2022: EHA

June 21, 2022
New and updated preclinical and clinical data presented by biopharma firms at the European Hematology Association Congress, including: Ascentage, Canbridge, Daiichi Sankyo, Iaso, Innovent Biologics.
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Syringe and COVID-19 vaccine vials as question mark

COVID-19 IP waiver on the line at WTO conference

June 14, 2022
By Mari Serebrov
A lot of eyes are on the World Trade Organization (WTO) Ministerial Conference taking place in Geneva June 12-15, as member countries try to reach a consensus on a proposal that would allow certain members to waive intellectual property (IP) rights on COVID-19 vaccines for at least three to five years.
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Acute myeloid leukemia illustration

Daiichi Sankyo’s quizartinib doubles overall survival in patients with newly diagnosed FLT3-ITD-positive AML

June 14, 2022
By Tamra Sami
Daiichi Sankyo Co. Ltd.’s quizartinib met the primary endpoint of overall survival in the pivotal phase III Quantum-First study, which tested the addition of quizartinib to chemotherapy vs. chemotherapy alone for adults with newly diagnosed FLT3-ITD-positive acute myeloid leukemia (AML).
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