This webinar will focus on the transformative role of AI in the pharmaceutical industry. In this 3-part session, our experts will guide you through the evolving AI ecosystem, showcasing real-world applications and strategies that are already delivering measurable impact across the drug development lifecycle. First, we will explore how AI-driven requirements mapping automates the alignment of diverse regulatory and operational standards with structured frameworks to support platform design and compliance. Next, we will learn how IQVIA Literature AI leverages intelligent agents to enhance the efficiency and accuracy of evidence synthesis. Finally, we will discuss how to assess and improve the trustworthiness of large language models for biopharma, focusing on reliability and confidence strategies.

This webinar is for you if:

• You have a fundamental understanding of AI and want practical examples of how it drives efficiency and improves patient outcomes
• You are seeking to navigate evolving AI regulations, streamline literature reviews using AI, and enhance the trustworthiness of large language models in life sciences
• You aim to deepen your understanding of AI’s capabilities and limitations to support its safe, effective, and compliant use in healthcare and pharmaceutical settings

If you are based in Americas or EMEA, please CLICK HERE to register.

If you are based in Asia-Pacific or Japan, please CLICK HERE to register.