Avicenna Alliance: enhanced knowledge, improved decisions, better outcomes
FULL MENU

Nonclinical Application Task Force

Nonclinical Application Task Force

BACK

Nonclinical Application Task Force

Mission: Promote use of in silico solutions to conduct smarter (3R’s) nonclinical studies

In silico
applications simulate real-world scenarios using computational models rather than physical experiments. Adopting nonclinical in silico applications offers several advantages in various fields, as cost-effectiveness, time efficiency, reduced dependency on animal testing, flexibility and iterative testing, risk reduction, data-driven insights, or reduced environmental impact, amongst others.

The new Nonclinical
In Silico Application task force is part of the In Silico Application (ISA) Working Group that aims to deploy in silicomethods 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 task force focuses on nonclinical applications and aims to promote use of
in silico solutions to refine, reduce or replace non-clinical studies.

Goals

  • Create an expert group among our members
  • Compile and review existing in silico solutions to reduce and refine nonclinical studies (e.g., selection of appropriate animal model(s), endpoints, time-points)
  • Promote in silico approaches to derisk nonclinical studies
  • Investigate how in silico approaches can help to ease nonclinical to clinical translation


Enrico Dall'Ara

Enrico Dall'Ara

Co-Chair of the Nonclinical Application Task Force

Enrico Dall'Ara is Full Professor at the Division of Clinical Medicine of the University of …

READ BIO
Julien Clin

Julien Clin

Co-Chair of the Nonclinical Application Task Force

Numalogics

READ BIO

NEWS

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.

News Don’t Miss Our Keynote with Dr. Bassil Akra – 28 April 2026, 2 pm CEST

Don’t Miss Our Keynote with Dr. Bassil Akra – 28 April 2026, 2 pm CEST

Dr. Bassil Akra, a visionary leader in European medtech regulation, will reveal how medical device and IVD rules are evolving.

News Avicenna Days (AAD) 2026

Avicenna Days (AAD) 2026

You’re invited… and yes, this party is free.

Sign up for our monthly newsletter!

Sign up for our monthly newsletter!

Fill in the fields you find below

Avicenna Alliance is an initiative of:

Avicenna VPH

© 2018-2026 Avicenna Alliance | powered by We Berry