Events
Whether attending a conference around the world or participating in our informative webinars, you’ll embark on a transformative journey into the TriNetX ecosystem. Discover how our end-to-end drug development solutions and real-world data technology drive groundbreaking research and better patient care. Gain valuable insights from industry thought leaders, connect with passionate professionals and explore the latest advancements in healthcare and life sciences. Don’t miss the chance to shape the future of clinical research with TriNetX. Book a meeting at an upcoming conference or register for a webinar today and be part of our global community dedicated to enhancing healthcare, advancing research, and pioneering innovation.
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Recent Conferences
Featured Webinar
Diversity in Clinical Trials: Using Real-World Data to Improve Trial Design and Advance Health Equity and Robust Evidence Generation
Featuring guest speakers from Sanofi and Clinical Trials Transformation Initiative, this webinar concluded 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 of: real-time access to diverse patient populations, advanced analytics and insights, and secure and compliant data sharing. Don’t miss this opportunity to gain valuable insights from industry experts and contribute to the ongoing dialogue on improving diversity in clinical trials.
Featured Webinar
Solutions to Amplify Your Clinical Real-World Data Research
Enrich your data and expand your research opportunities as part of a global community advancing safer and more effective therapies for better patient care.
Join us 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 published research and advance outcomes.
On-Demand Webinar Video Library
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.
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.
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.