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Meet us at BIO Asia-Taiwan

July 23-27, 2025
Taipei, Taiwan
Meet our experts at BIO Asia-Taiwan July 23-27, 2025 Taipei, Taiwan

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

  • Discover Taiwan’s innovation-driven biomed sector and Southern Star Research’s span in this region.
  • Gain insights from Southern Star Research’s clinical trial experienceand partnerships across Asia.
  • Access a fast-track approval system that doesn’t compromise on ethics or quality—no IND required to start clinical trials.
  • Take advantage of the 43.5% R&D Tax Incentive, creating substantial cost savings for offshore companies.

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:

  • A global platform for networking, technology exchange, and strategic partnerships
  • A space to foster regional collaboration and innovation
  • An investment summit promoting cross-border engagement
  • Satellite symposia to enhance visibility and insights
  • Recognition of achievements through industry awards

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.

Schedule a meeting

BIO Asia-Taiwan GF

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The Australian Advantage

Cost

Eligible organisations receive a 43.5% cash rebate on trial costs with the Australian Research & Development tax incentive.

Speed

Get you trial up and running in 8 weeks with streamlined ethics approvals and no need for an Investigational New Drug application.

Quality

World-class healthcare facilities and renowned experts ensure your data is accepted by international regulatory bodies like the FDA and EMA.

Come and meet us

Our team will be available throughout this event to discuss how we can support your research initiatives. Whether you’re looking to start a new project, save an existing one or simply explore new partnership opportunities, we’re here to help.

Dr David Lloyd

Managing Director

  • 30 years of research experience in academia, pharma & CROs
  • Advisor to the Australian Government on Clinical Research reforms
  • Prominent industry positions including Co-Chair of the R&D Taskforce
  • Appointed to NSW Dept of Health Early Phase Expert Oversight Committee
  • Previous member of several NHMRC committees overseeing clinical research

 

Jaehee Lee

Business Development

  • Business development, Sales & Client Relationship Management
  • Project management & coordination between stakeholders in multiple countries and departments
  • International collaboration and partnership building
Head Office:

L1, 1 Merriwa Street,

Gordon, NSW, 2072 Australia

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Specialist experience

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.