The Westin San Diego Bayview Hotel

Oct 16, 2025 7:00 AM - Oct 17, 2025 7:00 PM

400 W Broadway, San Diego, CA 92101, USA

Real-World Evidence Conference

Translating Insights into Real-World Value

Early Bird Rates Expire

05

DAYS

09

HOURS

39

MINUTES

05

SECONDS

Overview

Short Course: October 9 | Virtual

Conference: October 16-17 | In-Person

In an ever-evolving healthcare landscape, real-world evidence (RWE) has emerged as a pivotal tool for shaping regulatory and reimbursement decisions. Traditionally associated with post-market safety monitoring, RWE now plays a critical role throughout the entire product development lifecycle. It enables real-time data analysis to enhance our understanding of diseases, refine treatment approaches, and substantiate coverage decisions.

DIA’s Real-World Evidence Conference is designed to delve into the latest advancements and innovative applications of RWE. From data standards, new regulatory guidances, and advanced approaches for noninterventional studies to the role of RWD in clinical trial diversity, this conference will provide participants with cutting-edge insights into how RWE is transforming drug development and regulatory practices. By exploring new methodologies, technological advancements, and practical case studies, the event will equip attendees with the knowledge and tools necessary to leverage RWE effectively and drive forward healthcare decision-making. Don’t miss this opportunity to stay ahead in the field and harness RWE’s full potential to impact patient outcomes and policy.

Featured

Want to learn more about Real-World Evidence Conference? You've come to the right site!

Exhibits

Highlights & Features

Who should attend?

  • Conference Designed For:

    • Academia
    • Advocacy and Service Provider Professionals
    • Biopharma/Medical Device Industry
    • Clinical Research
    • Data analytics
    • Epidemiology
    • Health Authority
    • Health Economics and Outcomes Research
    • Payer
    • Pharmacovigilance
    • Policy
    • Real-World Evidence
    • Real-World Data
    • Regulatory Science
    • Technology Development

Short Course or Primer

To keep you at the forefront.

Oct 09, 2025

Short Course:

Getting Started with Estimands in Real-World Evidence Studies

Program Committee

  • Jaclyn  Bosco, PhD, MPH, FISPE
    Jaclyn Bosco, PhD, MPH, FISPE Vice President & General Manager, Global Head of Epidemiology & Database Studies
    IQVIA, United States
  • Alicia  Gilsenan, PhD, MS, RPh, FISPE
    Alicia Gilsenan, PhD, MS, RPh, FISPE Vice President, Epidemiology
    RTI Health Solutions, United States
  • Rachele  Hendricks-Sturrup, DrSc, MA, MSc
    Rachele Hendricks-Sturrup, DrSc, MA, MSc Research Director, Real-World Evidence
    Duke-Robert J. Margolis, MD, Institute For Health Policy, United States
  • Charles  Lee, MBA, MS
    Charles Lee, MBA, MS Executive Regulatory Science Director
    AstraZeneca, United States
  • Sarah  Martin, PhD, MS
    Sarah Martin, PhD, MS Senior Director - Global Regulatory Policy (Oncology)
    Eli Lilly and Company, United States
  • Keri  Monda, PhD, MS
    Keri Monda, PhD, MS Executive Director, Center for Observational Research
    Amgen, United States
  • Hetal  Pansuria
    Hetal Pansuria Vice President, Regulatory Affairs, Clinical Strategy and Ad-Promo
    Pacira Biosciences, United States
  • Motiur  Rahman, PhD, MPharm, MS
    Motiur Rahman, PhD, MPharm, MS Senior Epidemiologist, Real World Evidence Analytics, OMP, CDER
    FDA, United States

Digital Learning Catalog

DIA Learning: eLearning Soultions
Download

Have an account?

Be informed and stay engaged.

Don't miss an opportunity - join our mailing list to stay up to date on DIA insights and events.