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Southern Star Research at BIO China 2026

March 12-14
Suzhou, China

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.

Andy Hu

Director, Business Development

Southern Star Research (SSR) is excited to participate in BIO China 2026, one of Asia’s premier biotech and life sciences events. The conference brings together innovators, industry leaders, and global stakeholders to explore cutting-edge developments across biotechnology, pharmaceuticals, and healthcare.

Our Head of Business Development, Andy Hu, will be attending to connect with partners, share insights on clinical research innovations, and explore collaboration opportunities across the Asia Pacific region.

Visit us at the conference to learn more about SSR’s APAC presence and how we deliver tailored, end-to-end clinical research solutions across the region, including Clinical Development, Data Management, Medical Writing, Regulatory Affairs, and Pharmacovigilance.

Stay tuned for updates from the event and insights from our team on emerging trends in the life sciences sector.

Schedule a meeting

BIO China 2026

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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.

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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.