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Special Episode | Recording with BioSpace: Understanding the FDA’s AI Guidance in Pharmacovigilance episode artwork

EPISODE · Sep 19, 2025 · 25 MIN

Special Episode | Recording with BioSpace: Understanding the FDA’s AI Guidance in Pharmacovigilance

from The IQVIA Podcast · host IQVIA

In this episode, BioSpace’s head of insights Lori Ellis discusses the FDA’s first draft guidance for AI in drug development, published in January 2025, with Archana Hegde, Senior Director, PV systems and innovations at IQVIA.

What this episode covers

In this episode, BioSpace’s head of insights Lori Ellis discusses the FDA’s first draft guidance for AI in drug development, published in January 2025, with Archana Hegde, Senior Director, PV systems and innovations at IQVIA.

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Special Episode | Recording with BioSpace: Understanding the FDA’s AI Guidance in Pharmacovigilance

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Frequently Asked Questions

How long is this episode of The IQVIA Podcast?

This episode is 25 minutes long.

When was this The IQVIA Podcast episode published?

This episode was published on September 19, 2025.

What is this episode about?

In this episode, BioSpace’s head of insights Lori Ellis discusses the FDA’s first draft guidance for AI in drug development, published in January 2025, with Archana Hegde, Senior Director, PV systems and innovations at IQVIA.

Can I download this The IQVIA Podcast episode?

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