DIA 2025 Global Annual Meeting

DIA 2025 Global Annual Meeting

arrow_back View All Dates

11:00am EDT

Is Real-World Evidence Always a Last Resort?

11:00am EDT

From Approval to Access: Integrating Patient Insights into Coverage Decisions

11:00am EDT

Why do Good Clinical Practice Inspectors Do Things Differently and How can Approaches be Both Harmonized and Optimized

11:00am EDT

Accelerating Global Access to Drugs for Chronic Diseases

11:00am EDT

Project Orbis: Six Years Later

11:00am EDT

Unintended Consequences: Effects of Inflation Reduction Act on the Future of Pharmaceutical Innovation

11:00am EDT

Advancing Innovation Through Essential Drug Delivery Outputs

11:00am EDT

Putting Patients First: Leveraging Global Identification of Medicinal Products Standards to Strengthen the Drug Supply Chain and Improve Lives

12:50pm EDT

CH: Regulatory Intelligence to Drive Regulatory Strategy

2:15pm EDT

Expanding Innovative Master Protocol Trial Designs to Cell and Gene Therapies for Rare Diseases

2:15pm EDT

A Masterclass: Patient Recruitment Campaign Management

2:15pm EDT

Innovation at the Intersection: Clinical Operations, Data Management, and Quality Assurance on Quality-by-Design and Risk-Based Quality Management

2:15pm EDT

FDA Legislation 2025: How is Congress Preparing to Advance Innovation, Medical Product Safety, and FDA Funding?

2:15pm EDT

International Regulatory Harmonization for Development of Medicines: A Look at How far We’ve Come and Where We Go From Here

2:15pm EDT

Health Canada Town Hall

2:15pm EDT

Setting the Bar High: Facilitating Quality and Acceptability of Decision-Grade Real-world Evidence

2:15pm EDT

Best Practices for Navigating Divergent Regulatory Feedback

3:45pm EDT

Advances in Clinical Trial Linkage to Real-World Data: Bridging the Gap in Hybrid Clinical Trials

3:45pm EDT

Efficient Data Exchange: Drivers for End-to-End Standards Adoption

3:45pm EDT

Enhancing Evidence Generation Across Pharmaceutical Life Cycle: The Importance of Integrating the Patient Lived Experience

3:45pm EDT

How Soon is Too Soon? Enhancing Early Regulatory Engagement and Harmonization to Streamline Patient-Focused Drug Development

3:45pm EDT

Ethics in the Era of Precision Medicine and Advancing Technologies

3:45pm EDT

Integrating Clinical Trials and Clinical Care: The Who, What, When, Where, Why and How

3:45pm EDT

Applying Principles of Global Regulatory Collaboration to Address Chronic Disease

3:45pm EDT

FDA Accelerated Approval Program: Putting Withdrawals in Context

3:45pm EDT

WHO Town Hall: Driving Innovation and Access - Global Collaboration in Medical Product Regulation

3:45pm EDT

Unlocking the Future of Clinical Trials: How the ICH M11 Digital Protocol Template Enables Key Stakeholders

3:45pm EDT

Spinning Plates and Juggling Chainsaws: Mastering the Art of Complex Project Management

3:45pm EDT

Mastering the Power of Words: Elevate Performance and Compliance through Confident Communication

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