International Clinical Evidence Professional Society, the global leader in the development of innovative approaches to evidence harmonization for medical devices and in-vitro diagnostics.
Virtual Event
Introduction to In Silico and In Silico Clinical Trials, with Case Study Examples
October 22 @ 2:00 pm - 5:30 pm
Virtual Event
€35,00
Discover how computational modelling and simulation can support clinical evidence generation for medical devices.
22 October 2026 | 2:00 PM CET | Online
About the Webinar
In silico methods are playing an increasingly important role in the way clinical evidence can be generated and assessed for medical devices.
This webinar will introduce the principles of in silico methods and in silico clinical trials, exploring how computational modelling and simulation can complement traditional clinical evidence and contribute to regulatory decision-making.
Through practical examples and case studies, participants will gain a clearer understanding of how in silico approaches can be integrated into evidence-generation strategies and where they may bring value alongside clinical data.
The session will be presented by Martha De Cunha Maluf-Burgman, Leader of the Policy Development Working Group at the Avicenna Alliance, in the context of the Alliance’s advocacy work.
What We’ll Cover
During this 90-minute webinar, we will explore:
- The fundamentals of in silico methods and in silico clinical trials
- How computational evidence can complement traditional clinical evidence
- Current regulatory expectations for clinical evidence
- Practical case studies combining in silico and clinical data
- Emerging regulatory considerations
- Opportunities for incorporating computational approaches into evidence-generation strategies
The presentation will be followed by a live Q&A, giving participants the opportunity to raise their questions and discuss the topic directly with the expert.
Who Should Attend?
This webinar is particularly relevant for:
- Regulatory Affairs professionals
- Clinical professionals and clinical trial managers
- R&D scientists
- Medical device and IVD manufacturers
- Regulators and Notified Bodies
- Students and professionals interested in emerging approaches to clinical evidence generation
Why Attend?
As approaches to evidence generation continue to evolve, understanding how computational methods can interact with traditional clinical evidence is becoming increasingly relevant.
This session provides an opportunity to explore the potential of in silico trials, understand their place within the regulatory landscape, and see through practical examples how computational and clinical evidence can work together.
Join us online on 30 September 2026 and explore the evolving role of in silico evidence in medical device clinical research.
Speaker
Martha De Cunha Maluf-Burgman
Leader of the Policy Development Working Group, Avicenna Alliance
Practical Information
- Date: 22 October 2026
- Time: 2:00 PM CET
- Format: Online via Zoom
- Registration Fee: €15 for ICEPS members and 35€ for non-members (VAT excl.)
- Zoom Access: The Zoom link and connection details will be sent by email.
- Recording: The session will be recorded, and access to it will be only for ICEPS members.
Important Information
Please note that this event is a live Question & Answer session only.
The purpose of the session is to provide clarification and discussion on the implementation of Estimands. Participants will have the opportunity to ask questions and exchange directly with the expert speaker.
This session is not a training course, and participation does not provide a certificate of attendance, training completion, or certification.
Your Zoom access link is personal and may not be shared. Any participant not registered through ICEPS may be removed from the webinar without notice.