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News Avicenna Days 2026 has been a great success - Thank you all !!!

Avicenna Days 2026 has been a great success - Thank you all !!!

We would like to extend a heartfelt thank you to all the speakers and panelists who contributed to Avicenna Days 2026. Your presentations, insights, and discussions made a real difference, bringing depth, energy, and forward-thinking perspectives to the event.

News Be part of Avicenna Days 2026 — register to explore the future of in silico medicine with global experts

Be part of Avicenna Days 2026 — register to explore the future of in silico medicine with global experts

Join the voices shaping the future of in silico medicine - In 2026, the Avicenna Alliance celebrates a major milestone: 10 years of advancing in silico medicine — and you are invited to be part of what comes next.

News Infrastructure or Collaboration? Advancing In Silico Medicine Together

Infrastructure or Collaboration? Advancing In Silico Medicine Together

Avicenna Days (AAD) 2026 - The Research & Technology Working Group

News What does it take to turn in silico innovation into real impact for patients?

What does it take to turn in silico innovation into real impact for patients?

At AAD 2026, the ISA Working Group session brings together key voices from across the ecosystem to tackle exactly that question.

News Join us for a keynote teaser at  Avicenna Days (AAD) 2026

Join us for a keynote teaser at Avicenna Days (AAD) 2026

At Avicenna Days 2026, Prof. Oscar Camara, Director of the Engineering School at Universitat Pompeu Fabra (UPF), Barcelona, will explore how Virtual Human Twins are moving from long-standing vision to clinical reality.

News Harmonizing the Future: Global Regulatory Perspectives on In Silico Evidence

Harmonizing the Future: Global Regulatory Perspectives on In Silico Evidence

If we can submit in silico evidence for regulatory approval to the FDA, we still need to rely exclusively on clinical trial result to the rest of the world until regulation are harmonized! Really? Let's ask the question to the regulators.

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