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Validating AI & LLMs in GxP Use Cases

August 14, 2025
11:00 am
 EST
 • 
60
 mins
Recorded on 
August 14, 2025
 • 
60
 mins

AI is already reshaping personalized medicine, clinical trials, pharmacovigilance, and manufacturing—but most pharma and biotech teams are stuck trying to validate AI models with legacy tools built for deterministic software. The result? Slower innovation, unclear audit trails, and compliance headaches. In this rebroacast of one of most popular webinars, you will learn a practical framework for validating AI in GxP-regulated environments so your R&D and data science teams can move faster without sacrificing compliance.

What you'll learn

  • A step-by-step framework for AI validation in GxP-regulated environments
  • Risk-based approaches to managing AI bias, explainability, and traceability
  • Tools and automation strategies to streamline validation and regulatory approval
  • How to align AI governance with FDA, EMA, and evolving compliance standards

Who should attend

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Speakers

Gabriel Pascualy

Gabriel Pascualy

Director of Solutions
Formerly
Erez Kaminski

Erez Kaminski

Founder & CEO, Ketryx
Formerly

Head of AI, Amgen

Interested?

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