DIA 2025 Global Annual Meeting

DIA 2025 Global Annual Meeting

arrow_back View All Dates

8:30am EDT

Innovations in Signal Detection: Advancing Safety Signals with the READUS-PV Guidelines and Regulatory Updates TBD From Measuring to Modeling the Patient Burden: An Interactive Take on What Defines the Patient Experience in the AI-Age TBD Realizing Value Through Responsible AI in Clinical Development TBD Revolutionizing Medical Writing: Evaluating and Building the Assistive Technology Ecosystem TBD A Platform for Platforms? The Intersection of the Platform Tech Designation and Prior Knowledge TBD International Harmonization in Real-World Evidence: Recent Efforts, Barriers and Future Enablers TBD Japan Town Hall TBD MHRA Town Hall TBD Real-World Data Traceability: Challenges and Solutions When Generating Real-World Evidence TBD

10:30am EDT

The Globalization of Risk Management TBD The Need for a Multi-Stakeholder Collaboration to Modernize ICSR Management: How? Why? What? TBD Case Studies of Application of AI in Risk-Based Quality Management TBD Resilient Leadership: Overcoming Isolation and Adversity TBD Novel Framework and Case Study to Support Scientific Rigor: A New Community-Focused Model for Sustainable Clinical Trial Participation TBD Participant Compensation in Clinical Trials: Exploring Today’s Landscape and Unlocking Opportunities TBD Transforming the Project Management Role to Meet the Emerging Needs in Pharma: Extending Scope from R&D Focus to Launch Projects TBD FDA, MHRA, Health Canada Views on Data Flow: The Backbone of Effective Risk Assessments in Innovative Clinical Trial Design and Conduct TBD ANVISA Town Hall TBD Pathways to Innovation: Navigating Regulatory Expectations for AI Technologies in Drug Development TBD US and EU Orphan Drug Regulations: Shaping the Ecosystem for Rare Diseases TBD

11:40am EDT

CH: Using Digital Protocols to Unlock Efficiency and Accelerate Clinical Trials TBD

12:20pm EDT

CH: Diversity Action Plans - Listen, Learn, and Execute TBD

1:00pm EDT

CH: Navigating AI Regulation in Pharma - Global Trends, Compliance Challenges, and Harmonization Efforts TBD

1:45pm EDT

Real-World Evidence to Optimize Risk Minimization Programs: How to Move from Art to Science TBD Has Decentralized Trials Crashed, or Are We Just Getting Started? An Inflection Point for Clinical Operations in Oncology TBD Updating Ethics: What’s New (and why it Matters!) in the 2024 Declaration of Helsinki Revision TBD Reliable AI in Biomedical Settings: A Framework for Trust and Innovation in an Evolving Landscape TBD How Medical Writing Can Support Accelerating the Development of Rare Disease Therapies: Insights from the FDA’s START Program Pilot TBD Addressing Participation Burden in Clinical Trials: Evidence, Participant Feedback, and Signal Interpretation to Drive Impact TBD US Executive Orders: Impact on Precision Medicine and Diagnostic Development TBD Guerrilla Strategic Delivery TBD Embracing ICH E6(R3) with Risk-Based Quality Management TBD Harmonizing Data Quality Frameworks: Bridging Regulatory Perspectives TBD Pediatric Cluster Town Hall TBD China Town Hall TBD Harnessing Opportunities Through Inspection Reliance: A Path to Greater Efficiency TBD Statistical Challenges and Innovations in Small-Sized Clinical Trials Using Composite Endpoint TBD Charting New Courses: Reshaping Opportunities and Breaking the Expert Mold in Career Development TBD

4:00pm EDT

Advancing Premarketing Safety Analytics through FDA and Industry Partnerships TBD Overcoming Site Burden: Driving Adoption of Automation and End-to-End Integration TBD Opportunities for Innovation Under Fragmented Regulatory Framework for Clinical Development of Medicines and Diagnostics TBD Delivering Effective Business Transformations and How to Apply them to Drug Development TBD New Data and Insights on the Vendor Qualification Process in Drug Development TBD Pharmacovigilance Inspections Fireside Chat TBD Enhancing Global Access to Innovative Therapies: Regulatory Convergence, Harmonization, and Collaboration in Advanced Therapy Medicinal Products TBD Towards Instantaneous Regulatory Decisions and Better Predictability TBD Patient Engagement in Trial Design and the Evolving Landscape of FDA, EMA and Country Authority Guidance TBD Global Collaborative Review: Understanding Overall Control Strategy and Patient Benefit-Risk TBD Externally Controlled Trials in Clinical Development: Challenges and Mitigation Strategies TBD Getting the Work of Medicines Development and Manufacturing Done by Hook or by Crook: Attracting, Retaining and Developing Key Talent in the New World of Work TBD

Filter By Date

Jun 9 - 19, 2025

June 2025
Sun Mon Tue Wed Thu Fri Sat

1 2 3 4 5 6 7

8 9 10 11 12 13 14

15 16 17 18 19 20 21

22 23 24 25 26 27 28

29 30
Filter By Venue

Washington, D.C., USA

All

EH
TBD
Virtual
Filter By Type

00: Plenary

All
Forum

01: ClinSafety-PV

All
Forum

Session

02: ClinTrials-Ops

All
Forum

Session

Tutorial

Workshop

03: Data-Tech

All
Forum

Session

Tutorial

Workshop

04: MedAffairs-SciComm

All
Forum

Session

05: Patient-Impact-Product-Dev

All
Forum

Session

06: PersonalizedMed-ComboProd-Diagnostics

All
Forum

Session

Tutorial

07: ProjectManagement-StrategicPlanning

All
Forum

Session

Tutorial

Workshop

08: RD-Quality-Compliance

All
Forum

Session

Tutorial

09: Regulatory

All
Forum

Session

Tutorial

Workshop

10: RegCMC-Product Quality

All
Forum

Session

Tutorial

Workshop

11: Statistics-Data Science

All
Forum

Session

Tutorial

12: ProfDevelopment

All
Forum

Session

Tutorial

Workshop

13: Spotlight

All
Forum

Session

14: DIAmond

All
Forum

Session

15: Content-Hubs

All
Workshop

16: Community-Rounds

All
Session

17: Posters

All
Session

18: InnovationTheaters

All
Session

20: Short-Courses

All
Tutorial
Level

Advanced

Basic

Intermediate
Keyword

Advanced Analytics

Artificial Intelligence (AI)

Bioethics

Biomarkers

Cell and Gene Therapy

Clinical Trial Design

Diagnostics

Digital Technology

Global Perspectives

Non-CE

Patient Experience

Payers

Pediatrics

Rare Disease

Real-World Data (RWD) / Real-World Evidence (RWE)

Regulator Perspectives

Regulatory Collaboration

Regulatory Convergence and Harmonization

Regulatory Reliance

Student Programming
Timezone