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IQVIA TechIQ 2026

October 7, 2026 12:00 PM - 7:00 PM (EDT)

Description

This year, IQVIA TechIQ includes a dedicated Quality & Regulatory track focused on the practical considerations of implementing AI in regulated life sciences environments.

 

Taking place on the afternoon of October 7, the session, "Advancing GxP AI: Driving Quality, Safety and Commercial Performance," will examine how organizations are preparing for and governing the use of AI across Quality Management Systems (QMS) and Regulatory Information Management (RIM) processes.

 

The discussion will focus on the foundational elements needed to support GxP-compliant AI, including data governance, process standardization, validation, and risk management. Through a customer presentation, panel discussion, and product demonstration, attendees will hear different perspectives on how organizations are addressing regulatory expectations, managing AI-related risks, and building the controls needed to support quality, compliance, and patient safety.

 

Key topics will include AI governance, data integrity, regulatory readiness, validation strategies, and the role of AI in quality and regulatory operations.

 

This session is intended for senior quality, regulatory, and compliance leaders interested in understanding the considerations, challenges, and opportunities associated with adopting AI in regulated environments.

 

For more information and to view the full TechIQ agenda, visit here.

 

 

Additional details you will need to provide MassMEDIC based on the other event listings:

 

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Contact Information

IQVIA
Name: Miyuki Bryan
Email: miyuki.bryan@iqvia.com
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