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See What's Next in Clinical Trial Feasibility

Join TriNetX at SCOPE Europe 2026
Booth #68 | Barcelona, Spain | October 13-14, 2026

Discover how deeper, connected real-world data, including genomics, clinical notes, and AI-powered insights, can help clinical teams improve feasibility assessments, identify the right sites faster, and accelerate study success.

Meet with our experts at Booth #68

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Explore the Future of Clinical Trial Intelligence

Stop By Booth #68 to Learn More

Our team will be available throughout the conference to discuss how sponsors, CROs, and research organizations are using real-world data to improve study planning, site selection, patient identification, and research outcomes.

Genomics-Powered Research

Unlock richer patient insights and accelerate precision medicine research through federated genomics data integrated directly into the TriNetX platform.

Learn about Genomics
Clinical Notes Intelligence

Go beyond structured data by leveraging clinical notes to uncover critical patient insights not typically captured in coded records.

Explore Clinical Notes
AI Built on Better Data

Discover how TriNetX combines AI with one of the world’s largest federated real-world data networks to deliver actionable insights throughout the clinical trial lifecycle.

Explore AI Solutions
Data-Driven Site Identification

Identify high-performing sites, evaluate patient availability, and optimize site selection with confidence.

Explore Site Identification
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Featured Speaking Session

Feasibility Without Guesswork: How Deeper Data (and Genomics) Improves Feasibility and Site Identification with Confidence

Date: Tuesday, October 13, 2026
Time: 9:50 AM (25 Minutes)
Track: C4: Clinical Data Strategy and AI Innovation

Presenter: Samantha Eells

Clinical trial feasibility is often slowed by fragmented data and assumptions that can lead to protocol amendments, startup delays, and underperforming sites. In this session, learn how enriched real-world data, including genomics and clinical notes, can help teams evaluate protocol criteria more effectively, identify high-performing sites with eligible patient populations, and make faster, evidence-based decisions.

Key Takeaways

  • Improve protocol feasibility with deeper patient-level insights
  • Identify sites with greater confidence
  • Leverage genomics and unstructured data to uncover hidden opportunities
  • Reduce trial startup risk and accelerate execution
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Continuing the Conversation

Webinar: Feasibility Without Guesswork: Unlocking Genomic and Real-World Data for Faster Study Execution

Wednesday, November 04, 2026
11am EST – 60 min

If you can’t join us in Barcelona, or want a deeper dive after the conference, register for our upcoming webinar expanding on the concepts shared during Samantha’s presentation.

What We’ll Cover

  • Real-world examples of data-driven feasibility

  • Using genomics in protocol planning and site identification

  • How AI helps transform feasibility workflows

  • Practical approaches for improving trial execution

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