Dr David Lloyd
Managing Director
Managing Director
Director, Business Development
Southern Star Research is excited to attend the BIO Asia-Taiwan International Conference & Exhibition 2025, to be held in Taipei. The event is organized by the Biotechnology Innovation Organization (BIO) and Taiwan Bio Industry Organization (Taiwan BIO) and has gained popularity to become one of the top three global BIO events and Asia’s largest biotechnology platform. The 2025 conference promises an international podium for industry engagement, collaboration, and opportunity.
Southern Star Research is a full-service Australian CRO that holds a strong local and global presence and delivers customized support to early-phase biotech companies looking to grow, scale, and attract investment. Whether you’re an emerging biotech, investor, or a financial advisor, our team welcomes you to connect and collaborate.
Meet Southern Star Research’s Leaders at Bio Asia-Taiwan
Why Attend?
Join over 2,000 conference participants and more than 130,000 exhibition attendees,
and connect with more than 50 international investors. The event brings together key players from North America, Europe, and Asia across biopharma, diagnostics, MedTech, and digital health.
This five-day program features over 150 expert speakers and offers:
Meet us in Taipei from July 23–27 at Asia’s leading biotech event. Our leadership team will be on-site and available for meetings—complete the form below to connect.
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L1, 1 Merriwa Street,
Gordon, NSW, 2072 Australia
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Each member of our Leadership Team boasts an average of 30 years experience. Our clients have access to an extraordinary group of Clinical Research professionals, whose experience covers Multinational Pharmaceutical companies, Biotechnology, Medical Device, CRO’s, research institutes, Universities, Industry Associations & Government Bodies. Together, we ensure that every aspect of your unique and novel drug study clinical trial is handled with scientific precision, care, and foresight.
Our team has all of the tools, knowledge and experience to solve almost any issue that may arise during the complex clinical trial process.
We recognize that each study is unique and different and there are nuances that need to be resolved proactively.
Our advisory board of top-tier specialists in multiple therapeutic areas engage in the early stages from protocol design in constructive discussions to anticipate challenges and enhance study efficiency throughout the study.