Avicenna Alliance Webinar: “Ensuring the Quality of In Silico Evidence for Medical Devices”
How can we ensure that in silico evidence is credible, reliable, and fit for regulatory decision-making?
When: 10 November 2026, 5PM CET
Where: Online
As computational modelling and simulation become increasingly important in medical device development, establishing a common, risk-informed approach to model credibility is essential to supporting their wider regulatory acceptance.
Join the Avicenna Alliance monthly webinar to explore the updated In Silico Position Paper and its framework for generating, assessing, and using credible computational modelling and simulation evidence throughout the medical device lifecycle.
The discussion will address:
– Defining the question of interest and context of use
– Applying risk-informed credibility requirements and verification, validation, and uncertainty quantification (VVUQ)
– Addressing emerging challenges in AI-driven and hybrid models
– Ensuring data integrity, provenance, traceability, and reproducibility across computational and bioinformatics workflows
Featuring expert speakers:
Marc Horner, Thierry Marchal, Francesco Pappalardo, Martha de Cunha, and Ani Amar.
Whether you are a researcher, developer, industry professional, or regulatory stakeholder, this webinar will offer valuable insights into advancing the reliable adoption of in silico evidence in medical device development and evaluation.
Register here
