Risk assessment remains one of the most demanding stages of validation projects in Life Sciences. Large volumes of source material, complex system contexts and limited expert availability can make Functional Risk Assessment and process analysis highly time-intensive.
At the same time, regulated organisations are looking for practical ways to use artificial intelligence without compromising expert oversight, accountability or formal approval.
To explore what this can look like in practice, eLife Sciences is hosting a new webinar:
Validation of the Future: Automating FRA and Process Analysis with a Live LISC Demo
Date: 18 August 2026
Time: 11:00–12:00 CEST
Speakers:
Michał Timler, Validation Business Unit Director at eConsulting
Mateusz Macocha, Digital Transformation Advisor at eConsulting
This practical session will present a real-world Life Sciences use case and demonstrate how LISC Risk Assessment can support Functional Risk Assessment and process analysis.
Rather than discussing AI only at a conceptual level, the speakers will take participants through a large-scale risk assessment project, explain the analysed system and project assumptions, and show how the source materials were used within LISC.
Participants will see what this type of analysis would typically require in terms of time and expert involvement, what was achieved with LISC and how the platform helps transform dispersed project information into structured outputs ready for professional review.
From source materials to expert-reviewed analysis
LISC is designed to support the preparation and structuring of risk assessment work while keeping qualified experts fully responsible for evaluation, correction and formal approval.
During the webinar, participants will see how the platform works with project inputs and supports the transition from source documentation to a structured risk assessment.
The session will cover:
- a practical Functional Risk Assessment use case,
- the analysed system and its project context,
- the assumptions applied during the analysis,
- the input materials used within LISC,
- how the platform supports functional and process risk analysis,
- the structured output generated for expert review,
- the role of the qualified expert in verification and correction,
- the potential time and effort savings compared with a traditional workflow.
A live demonstration of LISC
A central part of the webinar will be a live demonstration of the platform.
The speakers will show how LISC processes the selected project inputs, supports the organisation of risk-related information and prepares structured material that can be reviewed and refined by an experienced validation professional.
The objective is not to remove experts from the process. It is to reduce repetitive preparation work and allow specialists to focus their attention on risk logic, project context and decision-making.
Beyond a single use case
LISC Risk Assessment is the first product within a broader platform being developed for regulated Life Sciences environments.
During the session, the team will also share the latest developments within LISC and present the evolving product roadmap. Participants will gain insight into how the platform is being expanded and how future use cases may support additional stages of validation and compliance work.
This webinar is part of a wider practical series. The next session will introduce another use case and demonstrate the next stage of LISC’s development.
Who should attend?
The webinar is designed for professionals responsible for quality, validation and risk-based decision-making in regulated Life Sciences organisations, including:
It will be particularly relevant for organisations exploring how AI-supported tools can reduce manual effort while preserving expert control and regulated decision-making.
Why attend?
Participants will leave the session with a practical understanding of:
- how LISC can support a real validation risk assessment project,
- what types of source materials can be used,
- how AI-supported preparation fits into an expert-led workflow,
- where time and effort may be reduced,
- how human review and formal approval remain embedded in the process,
- how the wider LISC platform is expected to develop.
Register for the webinar
Join us to see Functional Risk Assessment and process analysis demonstrated in a practical Life Sciences use case.
Date: 18 August 2026
Time: 11:00–12:00 CEST
Register here: [registration link]
