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Top Rated Electronic Data Capture Software with Non profits - Page 7

Last updated: September 2026

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154 software options

Clinion eSource logo
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Real-time e-source capture for clinical trials

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Clinion eSource enables site personnel to capture clinical trial data directly at the point of care through a secure mobile application. The software features automated data validation, maintains comprehensive audit trails with timestamps, and integrates seamlessly with electronic data capture systems in real time. It supports offline data entry with automatic synchronization and includes configurable user permissions for enhanced security.

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Trial Online logo
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Clinical trial management software

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Trial Online is a clinical trial management software that helps businesses set up role-based access rights, manage derived calculations, monitor compliance, handle patient diaries, conduct audits, and more from within a unified platform. It allows staff members to segment patients based on data collected via events and questionnaires. It also lets employees configure reminders, maintain logbooks, and automatically receive safety and non-conformance alerts.

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Nukleus logo
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Cloud-based electronic data capture platform

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Nukleus is an Electronic Data Capture (EDC) platform designed for clinical data collection in electronic format. It replaces traditional paper-based methods, streamlining the data collection process. The platform integrates coding libraries like MedDRA and WHO-DD ICD-10, enabling accurate coding of medication, medical history, and adverse event terms.

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ACTide eCRF logo
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eClinical data management platform for trials

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ACTide is an eClinical ecosystem and data management solution designed for clinical trial management across all study phases. The platform features integrated modules including electronic data capture, eCRF design tools, ePRO for patient engagement, eTMF for compliance, and CRA tools for data monitoring. It serves pharmaceutical, medical device, animal health, and nonprofit organizations with cloud-based capabilities for multicenter trials and regulatory submissions.

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