12 – 14 March 2026

BIO CHINA 2026

BIO CHINA 2026

12–14 March 2026 | Suzhou International Expo Center, Suzhou, China

Avance Clinical, a full‑service CRO with more than 30 years of experience, will attend BIO CHINA 2026, a premier gathering of global biotech innovators and scientific leaders.

Meet with us in Suzhou 12–14 March to learn how Avance Clinical supports faster, globally aligned clinical development through integrated early‑phase and multi‑region capabilities.

Seamlessly Scale with Avance Clinical

Our robust operational presence across Asia enables biotechs to run coordinated, multi‑region clinical programs across all phases.

For Chinese biotechs:

  • A clear pathway to global development beginning with rapid early‑phase clinical trials in Australia
  • Smooth expansion into North America and other key regions with aligned data and regulatory expectations
  • Reduced operational complexity through integrated program oversight

For North American and European biotechs:

  • A structured entry into China for cost‑efficient later‑phase studies
  • Access to large and diverse patient populations that support accelerated recruitment
  • Therapeutic expertise across oncology, metabolic, infectious, hepatic, renal, and CNS indications

At BIO China, discover how our Asia Advantage delivers speed, scalability, and global‑ready data quality, backed by the scientific and medical expertise that supports biotechs through every stage of early development.

A Leader in Australia Early‑Phase

Recognized as Australia’s leading early‑phase CRO, Avance Clinical supports biotechs with fast, globally aligned early‑phase development pathways. Australia’s clinical research environment provides several unique advantages, including:

  • Fast ethics approvals with first‑patient‑in possible in 5 to 6 weeks
  • No IND requirement, reducing early regulatory burden
  • Up to 43.5% R&D tax rebate on eligible clinical trial costs
  • Access to world‑class clinical sites and highly experienced investigators
  • High‑quality data accepted by global regulators including the TGA, FDA, EMA, and MHRA

Avance Clinical leverages these advantages to help biotechs reach proof‑of‑concept sooner, manage costs effectively, and transition smoothly into global later‑phase programs.

Meet Our Team at BIO CHINA 2026

Fred Li

Fred Li

Director of Business Development

Fred Li's LinkedIn Profile

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Jessica Han

Jessica Han

Director, Asian Operations

Jessica Han's LinkedIn Profile

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Connect with us

Connect with us during BIO CHINA to explore how Avance Clinical can accelerate your pathway from early‑phase trials to global development success.

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