DIA 2025 Global Annual Meeting

DIA 2025 Global Annual Meeting

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8:30am EDT

Electronic Submission of Safety Reports using E2B R3 standard - Ready for Primetime?

8:30am EDT

Newly Released Benefit-Risk Balance for Medicinal Products: A CIOMS Working Group XII Report

8:30am EDT

Expanding Research Participation through Local Health Care Providers: Perceptions and Strategies to Reach Communities

8:30am EDT

Tackling Fraud and Misconduct in Clinical Trials: Regulatory and Industry Perspectives

8:30am EDT

Building Upon Quality by Design and Risk-Based Monitoring Implementation Momentum

8:30am EDT

Global Integration of the Middle East Region: Growing, Developing and Benchmarking to Global Standards

8:30am EDT

The Role of Medical Device/IVD Regulatory Consulting in Navigating Complex Global Regulatory Pathways

8:30am EDT

How to Reduce Post-Approval Changes Complexity Through Agile Regulatory Reliance

8:30am EDT

Rare but Real: Navigating Rare Disease Product Development and Market Access Challenges

10:30am EDT

From Guidelines to Real-World Impact: Considerations for the Practical Implementation of ICH M14

10:30am EDT

Trustworthy AI Solutions for Next-Generation Pharmacovigilance

10:30am EDT

Partnerships and Collaboration: How to Drive Clinical Trial Success in Africa

10:30am EDT

Patient Referral: Is It Hope or Hype?

10:30am EDT

Delivering Business Value by Utilizing AI and Structured Content Authoring Tools in Regulatory Medical Writing

10:30am EDT

Why Patient/Site Collaboration is a Must Have to Ensure Accessibility to Digital Health Technologies and Development of Patient Relevant Clinical Endpoints

10:30am EDT

Why Does Drug Loss Occur? Challenges to be Addressed for Patients, and Japan's Contribution to Globalized Drug Development

10:30am EDT

Clinical Trial Innovation at Scale: Opportunities to Increase Adoption and Acceptance

10:30am EDT

Practical Implementation of MRCTs Based on ICH E17 Guidelines

10:30am EDT

Navigating the Challenges of Drug Delivery Using a Novel Device

10:30am EDT

Quality Oversight: Enhancing Approaches Across Organizations to Ensure Stable Product Supply and Timely Approval

10:30am EDT

Artificial Intelligence in the Medicines Lifecycle: Delivering Globally for Public and Animal Health

12:20pm EDT

CH: Addressing Key Challenges in Global Biosimilar Development and Regulation

1:45pm EDT

AI, Virtual Control Groups, and Organoids: How New Technologies are Being Developed to Align With Ethical Principles in Animal Research

1:45pm EDT

Clinical Development of Orphan and Pediatric Drugs, Along with Regenerative Medicine Products in Japan

1:45pm EDT

Post-Marketing Safety Management in Asia Using Real-World Data: Changes and Regulatory Harmonization with the US and Europe

1:45pm EDT

Techquity in Digital Trials: Tech, Data, and Operationalizing Equity in Clinical Research

1:45pm EDT

Portfolio Management in Pharma: Strategies and Insights from Large, Medium, and Small Pharma Organizations

1:45pm EDT

Pharmacovigilance Inspections: How Do Inspectors Decide Where and When to go?

1:45pm EDT

Africa's Evolving Regulatory Landscape

1:45pm EDT

EMA Town Hall

1:45pm EDT

Evolving Regulatory Considerations for Medical Affairs Communications

1:45pm EDT

Pharmaceutical Quality Knowledge Management Platform Supporting Global Regulatory Assessment: Regulatory and Industry Perspectives for Translating Vision to Implementation

3:00pm EDT

CH: Business Agility in the Age of AI - Why Zooming in Matters Just as Much as Zooming Out

4:00pm EDT

Enhancing Pharmacovigilance and Reducing Medication Errors by Applying AI to Product Labels

4:00pm EDT

Examining Bias in Lung Cancer Study Protocols: Lessons Learned from Multi-Stakeholders

4:00pm EDT

Cutting Through the Hype: How are AI and Emerging Technologies Accelerating Progress Now?

4:00pm EDT

Privacy-Preserving Data Access and Collaboration for RWE Generation Across Locations: Advances, Opportunities, and Challenges

4:00pm EDT

Collaborating for Equity: Reaching Communities Through Partnerships with Federally Qualified Health Centers and Community Health Workers

4:00pm EDT

Successful Patient Input to Regulatory and Health Technology Assessment Processes Along the Development Path: Examples of How to Optimize Impact

4:00pm EDT

Critical to Quality Assessment Reports from Inception to Operationalization: How to Engage Internal Stakeholders

4:00pm EDT

International Regulatory Engagement for Advancing Regulatory Science Approaches to Enable New Products to Address Patient Needs

4:00pm EDT

Beyond Weight Loss: Pioneering the Future of Obesity Drug Development

4:00pm EDT

FDA Rare Disease Town Hall

4:00pm EDT

Regulatory Perspectives on the Adoption of Advanced Manufacturing Technologies

4:00pm EDT

Modernizing Evidence in Oncology: Real World Data and Artificial Intelligence in Clinical Drug Development

4:00pm EDT

Beyond Clinical-Outcome Assessments: Best Practices for Submitting Other Types of Patient Experience Data to Regulators

4:00pm EDT

Business Agility: Recognizing Global Business Environment and Appropriate Strategies Adaptations

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Jun 9 - 19, 2025

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00: Plenary

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01: ClinSafety-PV

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02: ClinTrials-Ops

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03: Data-Tech

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04: MedAffairs-SciComm

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05: Patient-Impact-Product-Dev

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06: PersonalizedMed-ComboProd-Diagnostics

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07: ProjectManagement-StrategicPlanning

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08: RD-Quality-Compliance

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09: Regulatory

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10: RegCMC-Product Quality

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11: Statistics-Data Science

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12: ProfDevelopment

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14: DIAmond

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