Welcome back to another power-packed episode of the TMF Daily Podcast! I’m your host, Nicole Palmer, and today we’re diving into a game-changer for clinical trials—AI’s role in authoring regulatory documents.
Imagine a world where documents are streamlined, more accurate, and faster to produce… and it’s not all human hands doing the work!
But here’s the twist: with AI stepping in, we’re now asking the big questions—how do we regulate AI itself?
How do we ensure this technology is reliable, compliant, and meets the high standards the life sciences world depends on?
Joining me today is Edye Edens, and together, we’re pulling back the curtain on this double-edged sword. We’re talking risks, regulatory impacts, and how AI might just revolutionize the entire clinical trial process. Whether you’re in clinical research, regulatory, or just here to stay ahead of the curve, this episode has insights you won’t want to miss.
Let’s jump in! 🚀
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