DIA 2025 Global Annual Meeting

Agenda

Day 1 Jun 16, 2025

11:00 AM — 12:00 PM

A Regulator's View on the Future Vision for Pharmacovigilance

3:45 PM — 4:45 PM

Pharmacovigilance: Beyond Signal Detection and Spontaneous Reporting

Day 2 Jun 17, 2025

8:30 AM — 9:30 AM

Innovations in Signal Detection: Advancing Safety Signals with the READUS-PV Guidelines and Regulatory Updates

10:30 AM — 11:30 AM

The Globalization of Risk Management

10:30 AM — 11:30 AM

The Need for a Multi-Stakeholder Collaboration to Modernize ICSR Management: How? Why? What?

1:45 PM — 2:45 PM

Real-World Evidence to Optimize Risk Minimization Programs: How to Move from Art to Science

4:00 PM — 5:00 PM

Advancing Premarketing Safety Analytics through FDA and Industry Partnerships

Day 3 Jun 18, 2025

8:30 AM — 9:30 AM

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

8:30 AM — 9:30 AM

From Bedside to Bench to Bedside: How Adverse Events Converge Clinical Research and Clinical Care

8:30 AM — 9:30 AM

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

10:30 AM — 11:30 AM

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

10:30 AM — 11:30 AM

Trustworthy AI Solutions for Next-Generation Pharmacovigilance

1:45 PM — 2:45 PM

Addressing Challenges in Devices Safety Monitoring

1:45 PM — 2:45 PM

4:00 PM — 5:00 PM

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

Day 4 Jun 19, 2025

9:00 AM — 10:00 AM

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