NexaSource™

Fast, flexible eSource for clinical trials

Purpose-built for sites that need speed, flexibility, and simplicity ™ with rapid deployment and a clean, intuitive interface.

Built for coordinators, designed for clarity

Explore a sample study workspace ™ switch views below. Illustrative data only.

app.nexasource.io

Study dashboard

Last synced 2 min ago ™ All systems operational

Live SC
12Enrolled
3In screening
87%Forms complete
0Open queries

Upcoming visits this week

4 scheduled
SubjectVisitWindowStatus
1042ScreeningTodayIn progress
1038Week 4Thu 6/19Ready
1029Week 8Fri 6/20Ready

Subject roster

15 total
IDStatusLast visitCompletion
1042Screening72%
1038EnrolledWeek 4100%
1031EnrolledWeek 294%
1029EnrolledWeek 8100%
1017CompletedEnd of study100%

Screening visit ™ Subject 1042

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Overview

NexaSource™ is our purpose-built eSource platform designed for clinical research sites that need speed, flexibility, and simplicity. Built by the same team that supports leading sites across the country, NexaSource™ delivers a clean, intuitive interface and rapid deployment ™ helping sites move from paper to digital with minimal disruption.

Ease of use

  • Intuitive design: Coordinators and investigators can navigate forms effortlessly, reducing training time and errors.
  • Streamlined workflows: Built around how sites actually operate ™ visit schedules, source templates, and data entry flows are optimized for real-world use.
  • Minimal onboarding: Teams can begin entering data within days, not weeks.

Customization

  • Flexible form design: Every study can be tailored to its protocol ™ from visit structures to CRF logic.
  • Sponsor-specific configurations: NexaSource™ supports unique sponsor requirements without compromising site usability.
  • Built-in validation: Custom rules and edit checks ensure clean data capture from the start.

Rapid uptime

  • Two-week deployment: New studies can be live in as little as two weeks ™ including form build, testing, and go-live.
  • Dedicated support: Our team handles setup and validation so sites can focus on patient visits.
  • Scalable architecture: Designed to handle multiple concurrent trials without performance loss.

Why sites choose NexaSource™

  • Fastest path from protocol to live eSource
  • Seamless integration with existing EDC workflows
  • Proven reliability across multi-site deployments
  • Backed by Nexa Trials' hands-on clinical technology expertise

Get started

Whether you're moving off paper or scaling digital operations, we'll map a deployment path that fits your study portfolio.

Talk to our team

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Ready to go live on NexaSource™?

Tell us about your studies and timelines ™ we'll show you how fast your next trial can launch.

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