Validating AI System in Pharmacovigilance: Insights from the EU AI Act and EudraLex Draft Guidelines
In my previous post, I explored how AI is transforming pharmacovigilance and highlighted use cases that go beyond case intake. Building on that discussion, I wanted to understand how organizations are validating AI applications and what regulatory guidelines say about it. While numerous frameworks exist-issued by bodies such as the FDA, WHO, CIOMS Working Groups, EMA, and Health Canada-I focused my review on two key documents: The EU AI Act EudraLex - Volume 4 - Good Manufacturing Practice (GMP) guidelines (draft) These are highly relevant to pharmacovigilance systems and encapsulate most of the critical points from other guidance documents....