Where Simple Meets Powerful.

Manage your clinical research site, site network, CRO, or sponsor data with intuitive software systems and unmatched customer service.

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Maximize efficiencies, improve trial management, and reduce costs.

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Complion

Connecting Investigators & Sponsors to Compliance

Eliminate paper and redundancies as well as ensure on-demand monitor-readiness with top-tier eRegulatory/eISF solutions designed for ACMs, Sponsors, and CROs.

Accelerating Clinical Trials through Power of Data

Boost study success with the industry’s leading solution for pipeline management, study startup, metrics capture and intelligence – your key to site performance improvement.

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BLOG: BEHIND THE SOFTWARE

Negotiating Sponsor ReimbursEment for Site-based Technology​ - A Complete Guide for Clinical Research Sites

Negotiating Sponsor Reimbursement for Site-based Technology​ – A Complete Guide for Clinical Research Sites

Clinical research is undergoing a significant transformation, driven by the adoption of site-based electronic systems. As the industry shifts towards these advanced digital platforms, including virtual visits, telemedicine, and sophisticated data management systems, their value becomes increasingly evident. eClinical technologies are improving the efficiency of clinical trials and becoming integral to their success. Consequently, a growing

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Data Migration: Getting Started with RealTime Software Solutions

Data Migration: Getting Started with RealTime  Software Solutions 

Amidst industry movements like the site network consolidation trend, broader diversity in clinical trials, and the increasing complexity of studies, clinical research sites are navigating an environment that demands even greater operational agility. RealTime Software Solutions recognizes this evolving need and offers a comprehensive eClinical suite of solutions designed to improve site operations, streamline workflows,

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Clinical Trial Naming Conventions

Clinical Trial Naming Conventions: Refining Standards in Clinical Trial Management 

Clinical trials operate under a strict framework of regulations and compliance standards, reinforcing the importance of meticulous record-keeping. Well-documented cases such as Vioxx serve as reminders for clinical research sites and academic medical centers conducting clinical trials, highlighting the critical nature of maintaining impeccable organization and regulatory adherence. As the volume of data and documents

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