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Sheraton Philadelphia Downtown Hotel

Oct 24, 2024 7:30 AM - Oct 25, 2024 4:10 PM

201 North 17th Street, Philadelphia, PA 19103

Real-World Evidence Conference

Translating Insights into Real-World Value

Early Bird Rates Expire






Conference: October 24-25, 2024

In a market that is constantly adapting and adjusting to the needs of the healthcare field, real-world evidence (RWE) is becoming increasingly important for regulatory and reimbursement decision-making. Historically used for post-market safety monitoring, RWE is now integrated throughout the product development lifecycle, and has led to the real-time analysis of data to better understand and gain insights on disease, approaches to treatment, and how to substantiate coverage decisions.

DIA’s Real-World Evidence Conference will explore new, innovative applications of RWE, and deliver cutting-edge insights to leverage this knowledge to advance healthcare decision-making.

Located in the Sweet Spot of PA

Hosting our 2024 conference, the Sheraton Philadelphia Downtown offers a home away from home. During your stay, enjoy the 24-hour fitness center, easy access to local cuisine, historic landmarks and museums, and 30th Street Station just five minutes away.


Need Approval in Order to Attend?

Download and fill out our Justification Letter to demand to supervisor why this is a must-attend event.


Participant Testimonials

DIA RWE is the best RWE-related event I've attended - it has compelling speakers, strong education opportunities, and a great collective of attendees. – Nicholaas Honig, JD, Senior Regulatory Counsel, Aetion

Great meeting. Very strong content. Was a really efficient way for me to catch up on RWD/E happenings over the past year! – Meredith Zozus, PhD, Professor; Division Chief and Director, Clinical Research Informatics, University of Texas Health Science Center


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


Highlights & Features

Who should attend?

  • Conference Designed For:

    • Academia
    • Clinical Research
    • Data analytics
    • Epidemiology
    • Health Economics and Outcomes Research
    • Pharmacovigilance
    • Policy
    • Real-World Evidence
    • Real-World Data
    • Regulatory Science
    • Technology development

Program Committee

  • David  Martin, MD, MPH
    David Martin, MD, MPH Vice President, Global Head RWE
    Moderna, United States
  • Jaclyn  Bosco, PhD, MPH, FISPE
    Jaclyn Bosco, PhD, MPH, FISPE Vice President and Global Head of Epidemiology
    IQVIA, United States
  • John  Concato, MD, MPH, MS
    John Concato, MD, MPH, MS Associate Director for Real-World Evidence Analytics, OMP, CDER
    FDA, United States
  • Diane  Gubernot, DrPH, MPH
    Diane Gubernot, DrPH, MPH Epidemiologist
    US FDA, United States
  • Rachele  Hendricks-Sturrup, DrSc, MA, MSc
    Rachele Hendricks-Sturrup, DrSc, MA, MSc Research Director, Real-World Evidence
    Duke-Robert J. Margolis, MD, Center for Health Policy, United States
  • Camille  Jackson
    Camille Jackson Director, Regulatory Policy; Legal and Regulatory
    Flatiron Health , United States
  • Charles  Lee, MBA, MS
    Charles Lee, MBA, MS Executive Regulatory Science Director
    AstraZeneca, United States
  • Alexander  Liede, PhD, MSc
    Alexander Liede, PhD, MSc Senior Director, Global Epidemiology
    Abbvie, Ireland
  • Sarah  Martin, PhD, MS
    Sarah Martin, PhD, MS Senior Director - Global Regulatory Policy (Oncology)
    Eli Lilly & Co., United States
  • Brittany  McKelvey, PhD
    Brittany McKelvey, PhD Director, Regualtory Affairs
    Friends of Cancer Research, United States
  • Keri  Monda, PhD, MS
    Keri Monda, PhD, MS Executive Director, Center for Observational Research
    Amgen, United States
  • Representative Invited
    Representative Invited DIA, United States
  • Representative Invited
    Representative Invited DIA, United States

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