Embark on an exhilarating journey through the TriNetX Webinars – your gateway to a world of clinical real-world data research innovation! As your trusted guide, TriNetX collaborates with diverse healthcare partners, life science organizations, and critical stakeholders to unveil groundbreaking solutions that will transform the landscape of your research endeavors. Mark your calendar, register now, and join our global community in shaping the future of clinical research. Don’t miss the chance to navigate uncharted territories and discover the endless possibilities that await.

Upcoming Webinars

Diversity in Clinical Trials – Using Real-World Data to Improve Trial Design and Advance Health Equity and Robust Evidence Generation​

Join us for an insightful webinar that delves into the critical topic of diversity in clinical trials. This event aims to explore the use of real-world data (RWD) to enhance trial design, promote health equity, and foster robust evidence generation.


  • Moderator: Dr. Jeffrey Brown, Chief Scientific Officer at TriNetX and part-time Lecturer at Harvard Medical School, will moderate the discussion, bringing his expertise in clinical research and data analytics to the fore.

  • Panelists:

    • Dr. Sara Calvert, PharmD, Director of Projects at the Clinical Trials Transformation Initiative. Dr. Calvert will offer an overview of the current landscape of diversity in clinical trials, highlighting relevant regulations and initiatives aimed at improving inclusivity.

    • Beth Brooks, MPH, Head of Patient Insights and Behavioral Sciences at Sanofi. Beth will share practical use cases illustrating how Sanofi leverages RWD to design more inclusive clinical trials.

    • Dr. Jeffrey Brown, PhD, will delve into the intricacies of capturing diversity data in electronic health records and other systems. He will identify existing limitations in using RWD for diversity initiatives both in the US and globally, and discuss potential strategies to enhance RWD collection and utilization to support diversity goals.

The webinar will conclude with a dynamic 15-minute panel discussion moderated by Dr. Jeffery Brown, allowing attendees to engage with the speakers and delve deeper into the presented topics.

Don’t miss this opportunity to gain valuable insights from industry experts and contribute to the ongoing dialogue on improving diversity in clinical trials.

June 3, 2024


12:00 PM EDT

Zoom Webinar

On-Demand Webinar Video Library

Closing the gaps in multiple myeloma with Data and AI. Three speakers listed (Michael Sankey, Databricks; Jeffrey Graham, TriNetX; Luis Arthur Pelloso, MD, PhD, PPD) November 14, 2023 at 11:30 am ET

Closing the Gaps in Multiple Myeloma with Data and AI

Join real-world experts at TriNetX and Databricks as we examine how rich and timely clinical data, unified in a research-ready environment, can provide clinical researchers with the best opportunity to accelerate time-to-insight and influence outcomes.

Answering Questions & Making an Impact: Publishing with TriNetX Real-World Data

TriNetX is a go-to tool for researchers across the globe to conduct real-world evidence studies and find answers to their clinical questions. Our intuitive platform and rich, deep EHR data has enabled success for thousands of researchers and has appeared in over 700 publications since 2017.

Building Your Rare Disease Cohort with Real-World Data

“Rare” is relative. Today roughly 30 million patients in the U.S. live with a disorder characterized as rare by the FDA. Globally, hundreds of millions more fall into a similar category. In many cases, the course of their disease is poorly understood, and existing treatments – if they exist at all – are inadequate. Solving these problems starts with better research. And better research starts with the right cohort.

TriNetX Summit Recordings

TriNetX’s end user conference took place on October 17-19, 2022 at the InterContinental hotel in Boston. The two-day, invitation-only event brought the global community of TriNetX members together to network, share best practices, participate in training, highlight research discoveries and guide the company’s product roadmap including design, enhancements and development timelines.

Watch sessions and experience the innovation and excitement of the 2022 TriNetX Summit.

Flashlight illuminating night sky overlaid with data programming

Real-World Evidence Generation: A Model Process

Featuring TriNetX Chief Scientific Officer and FDA Sentinel System co-architect Jeff Brown, PhD, the webinar shows how LUCID connects the industry’s largest federated network of EHR and claims data to a high-performance data science environment.

Going Beyond the Limits of Legacy Pharmacovigilance with Real-World Data

The revolution in drug safety data is underway. The advent of RWD, together with technologies to aggregate, standardize, and analyze it, have turned Pharmacovigilance (PV) specialists into evidence generation leaders.

Follow the Patient: Prospective Monitoring with Real-World Data

What if you could combine the richness and volume of real-world data with the objectivity of prospective monitoring? Now you can. By tagging a cohort in TriNetX for active surveillance, you can “enroll” de-identified patients from around the world into a virtual study – in days, if not immediately – then monitor new data for those patients as it arrives.

From Detection to Action: Applying Your Model to Real World Data from TriNetX

From simple scoring formulas to regressions trained with machine learning, data models help us detect patients who may benefit from close monitoring, or who might qualify for a clinical trial. See the solutions we’ve developed to help researchers move from “detection to action” more efficiently over our global research networks.

Improving Access to Clinical Trials for Underrepresented Patient Populations Using Real-World Data and TriNetX’s Diversity Lens

Evaluate the impact of eligibility criteria on your trial’s enrollment of underrepresented patient populations. With these results, study teams can better adjust criteria and seek out partner organizations caring for the patients who qualify for their study.

Publishing with TriNetX: Guidelines, Best Practices, and a Real-World Example

Spend time with two experienced members of the TriNetX team and a recent author from Penn State College of Medicine to learn how to maximize your chances for successful publication at every step along the journey, from query design to corresponding with journal editors.

Closing Gaps in Patient Diversity Within Clinical Trials Using Real-World Data

Learn how to use real-world data on the TriNetX platform to explore patient diversity, identify gaps, and attain guidance to recommend and improve diversity in clinical trials and investigator-initiated studies.

Tokenizing and integrating patient data

Revealing the Patient Journey with Linked Claims and EHR

When it comes to patient journeys, EHR and claims each tell only half the story. Make sure you draw your insights from data that integrates the richest versions of each.

Introducing the Japan Claims Network

Trials that include patients in Japan have an advantage when it comes to regulatory approval in that country. But approval requires promising results from a well-executed study. Start the process the right way by understanding Japan’s patient population, designing a feasible study, and selecting the right trial sites.