News & Milestones

Setting the Global Standard in Organ-on-Chip Innovation

Key milestones in Anivance AI's journey to becoming Taiwan's leading organ-on-chip company and a globally recognized leader in regulatory-aligned drug development.

🏆 Landmark Achievement2025

Anivance AI Selected for FNIH NAMs Global Pilot Program — First from Taiwan

Our inhalation lung-on-chip platform was selected for the Foundation for the National Institutes of Health (FNIH) New Approach Methodologies (NAMs) global pilot program. Out of 64 proposals submitted worldwide, only 4 were selected — and Anivance AI is the first company from Taiwan to achieve this distinction.

4
Selected Globally
64+
Proposals Submitted
1st
From Taiwan

Why This Matters

  • Validates organ-on-chip technology for regulatory-grade inhalation toxicity assessment
  • Closely linked with FDA/NIH regulatory science frameworks
  • Establishes Anivance AI's lung-on-chip platform within the global regulatory validation pathway
Read on GBI Monthly

About Anivance AI's Organ-on-Chip Technology

Anivance AI (久浪智醫) is Taiwan's leading organ-on-chip company, specializing in AI-driven microphysiological systems (MPS) for regulatory-aligned drug development. The team was formed in 2021 by Dr. Guan-Yu Chen and officially incorporated as Anivance AI in June 2024. The company has rapidly emerged as a global innovator in

The company's flagship lung-on-chip platform simulates the human air-liquid interface and respiratory exposure environment, enabling high-fidelity inhalation toxicology testing without animal models. This technology was validated through selection into the FNIH NAMs (New Approach Methodologies) global pilot program — a landmark achievement for organ-on-chip technology from Taiwan.

Beyond inhalation toxicology, Anivance AI's platform supports multi-organ modeling including liver, CNS, immune system, and tumor microenvironment, with integrated AI analytics for high-throughput phenotypic analysis and predictive modeling. The platform is designed for IND-enabling preclinical studies and regulatory submissions to the FDA and EMA.

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