DIA 2026 Global Annual Meeting

DIA 2026 Global Annual Meeting

TBD

1:00pm • 12P : Real-World Evidence for Regulatory Decision-Making: Guidance, Methods, and Case Studies

105AB

107AB

4:00pm • #459: Bias and Methodological Challenges in External Control Arms Addressing Time-Related Bias, Endpoint Alignment, Unmeasured Confounding

108A

11:00am • #403: Clinical Operations in Transition: Leadership Perspectives on AI, the Workforce, and the Future of Trial Execution
2:30pm • #431: Expanding Access and Engagement: Lessons from Decentralized Clinical Trial Solutions
4:00pm • #446: DIA2026-001: Co-Creating the Patient-Centric Trial Live

108B

109AB

110A

11:00am • #416.1: International Regulatory Cooperation with the African Medicines Agency

111AB

112AB

115AB

115C

116

117

118AB

118C

201AB

202AB

203AB

204AB

Ballroom AB

8:00am • #400: Hidden Potential: Turning Today’s Science into Tomorrow’s Cures

Content Hub

Exchange

12:15pm • #418 POS: Student Poster Session I

Innovation Theater 1

Innovation Theater 2

Innovation Theater 3

Spark Stage

Zone A

1:00pm • #423 RT: Roundtable Discussion: Enhancing Regulatory Collaboration through Cloud Technologies

Zone B

1:00pm • #422 RT: Roundtable Discussion: Accelerating US Based Domestic Manufacturing by Leveraging Innovative Regulatory Concepts

103A

105AB

107AB

108A

108B

109AB

111AB

112AB

114

8:00am • #500: Transforming Obesity Patient Care: Past, Present, and Future Innovation in the Age of GLP-1 Therapies

115AB

115C

116

117

118AB

118C

4:15pm • #555: Adapting Regulatory Frameworks to Address Mass Distribution of Unapproved or Unauthorized Medicines

119AB

201AB

202AB

203AB

204AB

Content Hub

11:40am • #521 CH: Achieving Representative Enrollment in Phase 3 Lupus Clinical Trials: A Case Study

Exchange

11:30am • #520 POS: Professional Poster Session II

Innovation Theater 1

Innovation Theater 2

Innovation Theater 3

9:15am • #501 IT: Weave Bio Innovation Theater: Threading AI Throughout the Drug Development Lifecycle - An Enterprise Lens

Spark Stage

11:45am • #521.1 SS: Spark Stage: Patient Appreciation Session: Celebrating the Patient Voice

Zone A

Zone B

3:15pm • #544 RT: Roundtable Discussion: Is Your AI Ready to Scale? Build the Governance Backbone for Reliable Innovation and Trust

102AB

10:15am • #612: Achieving Regulatory-Grade Pragmatism in Streamlined Trials Embedded in Clinical Practice

103A

105AB

107AB

108A

108B

109AB

111AB

112AB

114

8:00am • #600: From Breakthrough to Life: Engineered T-Cells, Patients, and the Future of Biotech

115AB

116

117

118AB

118C

119AB

201AB

202AB

203AB

204AB

10:15am • #615: Navigating the FDA Commissioner's National Priority Voucher Program: Implementation Insights and Strategic Impact

Content Hub

Exchange

11:30am • #617 POS: Professional Poster Session III

Innovation Theater 1

9:15am • #601 IT: Faro Health Innovation Theater: Digital Protocols in Action - Enabling End-to-End Automation in Clinical Development

Innovation Theater 2

9:15am • #602 IT: PhaseV Trials Innovation Theater: From Protocol to Submission - The Real-World Impact of AI in Clinical Operations

TBD

Zone A

12:30pm • #621 RT: Roundtable Discussion: International Regulatory Cooperation with the African Medicines Agency

Zone B

12:30pm • #620 RT: Roundtable Discussion: Can You Complete Your Submission in 10 weeks?

102AB

8:00am • #708: Patient Preference Studies in Clinical Trial Design and Submissions: Enhancing Patient-Centricity with Insights from ICH E22

103A

8:00am • #701: No Report Left Behind: Human-Centered Safety Reporting

105AB

8:00am • #704: The View from the Top: What is the Future of Medical Writing?

107AB

8:00am • #710: Regulatory and Industry Perspectives on Good Clinical Practice Inspections: Regulatory Approaches, Industry Impact, and Future Harmonization Opportunities

108A

8:00am • #705: Fighting Medical Disinformation (Without Actually Starting a Fight)

109AB

8:00am • #702: Cross-Functional Agentic End-to-End Dossier Preparation: Where are we Today and Progress Towards Realizing the Vision

111AB

8:00am • #703: How RA/QA Leaders can Optimize AI and Reduce Risk as Industry Moves from the Wild West to its Inevitable Second Phase - Categorization

114

116

8:00am • #711: Role of External Data in Confirmatory Clinical Trial: Current Landscape and Future Perspectives

117

8:00am • #709: PV Compliance DIY: How to Find and Fix Quality Issues Before They Find You

118AB

8:00am • #700: Insights Regarding Implementation of the ASAP Process

118C

8:00am • #706: AI-Enabled Structured CMC Submissions: Leveraging Cloud Technology for Enhanced Collaboration and Analysis

DIA 2026 Global Annual Meeting

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