Live Webinar
AI in Pharma: Compliance, Regulations & GxP Boundaries
Your roadmap to safe AI adoption: Regulations, risk management, and guidelines
March 17, 2026 | 10 AM ET | Microsoft Teams
AI is transforming Pharma and MedTech, but compliance defines the boundaries. As regulations evolve, the key question is: How and where can AI be leveraged safely within the context of your business processes?
In this webinar, experts from Cegeka and Epista cut through the complexity to explain upcoming regulations, risk assessment principles, and human-in-the-loop safeguards. We’ll share practical examples, including Cegeka’s Quality Impact Recall Agent, and outline the do’s and don’ts for AI in regulated environments.
Join us to learn how to balance innovation with regulatory rigor.
What you'll learn:
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Upcoming regulations shaping the use of AI in pharma
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How to apply risk assessments and “human-in-the-loop” safeguards
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Practical, compliance-driven use cases, including Cegeka’s Quality Impact Recall Agent
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Key do’s and don’ts for using AI in regulated environments
Speakers
Thomas Van Dorpe - AI & ERP Solution Architect at Cegeka
Henrik Walther Madsen - Business Development Executive at Cegeka
Henrik Johanning - Senior Vice President at Epista
Register now!
Digital Innovation in Pharma & MedTech
Discover the full webinar Series
This webinar is part of our Digital Innovation in Pharma & MedTech series, designed to help industry leaders turn disruption into opportunity. Join us to tackle the most critical challenges shaping Pharma and MedTech today, from AI adoption and compliance to ERP validation, data integration, global roll-outs and supply chain resilience.
We believe in shaping digital together. We don’t just deliver technology, we work shoulder to shoulder with our clients to ensure technology drives impact when and where it matters most.
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