NexaSource™
NexaSource™ is an easily configurable eSource platform for clinical research sites. Designed to get a study up and running within two weeks — without high enterprise licensing costs, months-long IT projects, or forms that fight how coordinators actually work.
Explore a sample study workspace ™ switch views below. Illustrative data only.
Last synced 2 min ago ™ All systems operational
| Subject | Visit | Window | Status |
|---|---|---|---|
| 1042 | Screening | Today | In progress |
| 1038 | Week 4 | Thu 6/19 | Ready |
| 1029 | Week 8 | Fri 6/20 | Ready |
| ID | Status | Last visit | Completion |
|---|---|---|---|
| 1042 | Screening | ™ | 72% |
| 1038 | Enrolled | Week 4 | 100% |
| 1031 | Enrolled | Week 2 | 94% |
| 1029 | Enrolled | Week 8 | 100% |
| 1017 | Completed | End of study | 100% |
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What it is. NexaSource™ is a purpose-built, cost-effective eSource platform for clinical research sites. It delivers protocol-aligned digital source capture with flexible form configuration, built-in validation, and a clean interface coordinators can learn quickly.
What it solves. Enterprise eSource is often expensive, slow to configure, and overbuilt for site needs. Paper source creates duplicate entry, query risk, and audit headaches. NexaSource gives sites a practical middle path: digital source that fits the protocol, matches site workflows, and integrates with your existing EDC — without the cost and complexity of a full enterprise rollout.
How fast you go live. Nexa Trials handles form build, testing, and go-live support. Most studies are up and running within two weeks of kickoff, so your team can focus on patient visits instead of waiting on technology.
Whether you're moving off paper or scaling digital operations, we'll map a deployment path that fits your study portfolio.
Tell us about your studies and timelines ™ we'll show you how fast your next trial can launch.
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