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In Silico Application (ISA) Working Group

In Silico Application (ISA) Working Group

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In Silico Application (ISA) Working Group

Digital evidence can and must be used for regulatory approval in all parts of the world. The Research & Technology Working Group has made huge progress, which now allows to start applying modeling and simulation, as properly defined, to accelerate medical innovation access to patients.

Many organizations are willing to invest in in silico but practical implementation guidance is needed.

The new Avicenna In Silico Application (ISA) Working Group aims to deploy in silico methods downstream and design comprehensive solutions (process, access to research, software, hardware, humanware, possibly services) to allow any organization to time and cost effectively adopt and deploy in silico methods all along the development, registration and life cycle of the products.

The key goals of this group are:

  • Deploy in silico methods to optimize and streamline product quality and manufacturing through the product life-cycle.
  • Regulatory: Identify and address the challenge to deploy Computer Modelling and Simulation & Artificial Intelligence to refine, reduce or replace animal studies and clinical trials.
  • Promote and implement in silico medicine in healthcare, including clinical diagnostics (e.g., clinical decision support tool and AI-powered pathology), “proactive” vigilance.
  • Engage with reimbursement entities to understand, recognize and request the integration of in silico methods for healthcare

Priorities 2025 - 2027 and beyond:

2025:

  • Demonstrate added value of in silico approaches in CMC: from early stage (tech transfer) up to post-market (lifecycle);
  • Evaluate the use of in silico approaches in nonclinical development;
  • Assess current application of in silico approaches in clinical setting (in development and beyond).

2026:

  • Position paper(s): mapping of the current added value of in silico approaches in product life-cycle and clinical use
  • Promote implementation of in silico approaches (with R&T WG and Int. WG);
  • Educate stakedholders via position paper(s) and/or webinars.

2027 and beyond:

  • Sustain in silico advocacy for Medicinal Devices, Pharmaceuticals & other HealthTech products.

Cécile Rousseau

Cécile Rousseau

In Silico Application Working Group Leader

Senior Director, Nonclinical & Early Clinical Development, VCLS

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Emmanuelle Voisin

Emmanuelle Voisin

In Silico Application Working Group Leader

Founder & CEO, Voisin Consulting Life Sciences (VCLS)

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NEWS

News Avicenna Alliance at RAPS meeting in Pittsburgh

Avicenna Alliance at RAPS meeting in Pittsburgh

On October 8th, various key members of the Avicenna Alliance including Marc Horner, International Affairs WG leader, Martha de Cuhna, Policy Development WG Leader, and our new partner Surash Surash from the leading Notified Body TüV SüD, spoke at the Regulatory Affairs Professional Society (RAPS) meeting in Pittsburgh to highlight the essential and increasing role of in silico methods throughout the total product life cycle of medical devices.

News Avicenna Alliance Welcomes the Notified Body TÜV SÜD as a New Partner

Avicenna Alliance Welcomes the Notified Body TÜV SÜD as a New Partner

The Avicenna Alliance is delighted to welcome TÜV SÜD as its newest Partner. TÜV SÜD is a leading Notified Body operating across multiple regulatory territories, including the EU, the United States, the UK, and Asia. With more than 150 years of experience, a presence in 1,000 locations worldwide, and over 30,000 employees, TÜV SÜD is a trusted global partner in testing, inspection, certification, and training solutions.

News The Alliance at the iSi Health Symposium

The Alliance at the iSi Health Symposium

On 11 and 12 September 2025, our partner iSi Health, Erica Beaucage-Gauvreau and Rocio Castro Vinuelas, organised an excellent symposium in Leuven to bring together key players in the in silico community and promote networking, brainstorming and exchanges.

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