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Event date: 24/06/2026 15:00 - 16:00 Export event
Are you interested in AI Validation? Join our webinar on June 24th 2026
As generative and agentic AI become part of pharmaceutical operations, how do we validate these systems in a practical way? Generative and agentic AI are already in clinical trial operations, but the validation rulebook hasn't kept up. CSV and CSA were built for software that behaves predictably, not for systems that produce novel outputs and act before anyone reviews them. "Human in the loop" isn't a validation strategy: the April 2, 2026 FDA warning letter on AI over-reliance showed human review can be present and still fail.
Join us on Wednesday, June 24th for a webinar exploring the future of validating AI-enabled software. The session will identify key challenges, discuss practical, risk-based approaches, and talk about next steps. Our goal is to bring together cross-industry experts in an ongoing working group to build one practical, risk-based framework. If you're interested in contributing your expertise and helping shape the discussion, join the webinar on June 24th 2026, 10am EDT.
A registration link was sent out in this month's newsletter. If you haven't received it and are interested in participating, write jana.summa@eclinicalforum.org
Europe/Hybrid Autumn Workshop, October 27-29, 2026, Zurich, Switzerland, hosted by BSI Software
eCF Webinar November: FDA warning letters for audit trail analytics
FDA warning letters tell us what went wrong, but what could your audit trail analytics program have caught earlier? Join our upcoming webinar for a practical, in-depth look at an FDA warning letter and learn how to identify missed signals, uncover blind spots, and strengthen your audit trail review program.