Technological advancements and adoption in clinical trials continue to reshape the way data is collected, managed, and analyzed by clinical research sites, sponsors and CROs. Over the last decade, Electronic Source (eSource) has gained prominence for enabling direct data entry by investigators, reducing transcription errors and enhancing data quality. However, eSource in clinical trials is … Read more
The operating model for clinical research is shifting. Protocols are becoming more complex — more endpoints, more procedures, more oversight. In tandem, clinical research site networks and multi-site organizations are scaling rapidly, expanding across more studies, more sites, and more complex portfolios. But execution hasn’t kept pace. While trial complexity has accelerated, operational visibility has not. For sponsors and CROs, … Read more
Clinical research sites rarely struggle with opportunity. What they struggle with is capacity. Clinical research coordinators (CRCs) are buried in regulatory binders, monitors occupy office space for days at a time, and the sheer volume of manual transcription creates a hard ceiling on growth. A site may have the investigators, the patient population, and even … Read more
Why manual transcription from eSource to EDC is now the industry’s biggest and most fixable bottleneck. Clinical trials are entering a new era of technology innovation and adoption. We’ve seen AI-assisted site selection, decentralized models, real-time analytics, and fully digital workflows. Yet one of the most time-consuming, error-prone, and universally hated tasks in research has barely changed at all. Since the day eSource entered … Read more
Watch the Replay: The RealTime Keynote – The Next Chapter of eSource Every coordinator knows the drill: collect the data once, type it again, fix the errors, and reconcile the queries. It’s a burden that has never truly been solved – eSource to EDC. And for decades, clinical research has accepted the contradiction of collecting … Read more
Breakthrough interoperability feature, EDC Connect, eliminates redundant workflows between eSource and EDC systems—redefining how clinical trial data moves. SAN ANTONIO, TX — November 20, 2025 — RealTime eClinical Solutions today announced the official launch of EDC Connect, a breakthrough feature that eliminates duplicate data entry between eSource and Electronic Data Capture (EDC) systems, one of clinical research’s most persistent inefficiencies. The launch marks a major milestone … Read more
RealTime Reports: Closing the Gap Between eSource Data Capture and Data Flow. Modern sites are under relentless pressure: more trials, tighter timelines, higher expectations for data integrity, and audit readiness. Traditional paper-based or hybrid workflows simply can’t keep up. Electronic source data capture (eSource) is now rapidly becoming the gold standard for high-performing sites. In the latest … Read more
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This edition of RealTime Reports presents the findings from a survey of 255 clinical research professionals. The analysis reveals the current, site-level view of the real ROI of eSource.
eSourceOne The eSource solution engineered specifically for Phase 1 Clinic operations. Phase I clinics demand precision. High-volume subjects. Tight protocols. Split-second timing. And no room for error. Introducing eSourceOne, a Phase 1 clinic automation solution that delivers the control your site needs to support regulatory-compliant studies in the most complex early-phase environments. Get Insider Updates Built … Read more
