WHITEPAPER
AI in Drug Discovery: A Review of US & EU Policy Guidance
Global regulatory perspectives shaping the future of AI-driven pharmaceutical innovation.
Navigating Policy to Unlock AI’s Full Potential in Drug Discovery
Artificial intelligence is transforming drug discovery — accelerating timelines, improving accuracy, and enabling novel therapeutic development. This whitepaper reviews the latest US and EU policy guidance, including the FDA’s evolving AI/ML framework, the EU AI Act, and EMA’s recommendations, providing life sciences organisations with a roadmap for responsible and effective AI adoption.
Download the whitepaper to:
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Understand how AI is reshaping the drug discovery process from molecule design to repurposing.
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Learn about US regulatory initiatives, including the FDA’s AI/ML Action Plan and forthcoming guidance.
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Explore the EU AI Act and EMA’s human-centric approach to AI in medicine development.
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See how global AI safety initiatives are influencing healthcare innovation.
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Discover how to align AI-driven R&D with ethical, legal, and compliance standards.