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

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

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.
RealTime Solutions for Sites and Networks

SITES & NETWORKS

Try one system or bundle them all for a complete Site Operations Management System (SOMS)

RealTime Solutions for Sponsors and CROs

Maximize efficiencies, improve trial management, and reduce costs.

Your success is our success

Top rated CTMS on Capterra!

View study documents, refer patients,
sign documents with your fingerprint and more!

BLOG: BEHIND THE SOFTWARE

Solutions for the top 5 pain points for clinical research sites

Solutions for the Top 5 Pain Points for Clinical Research Sites 

According to a review from the National Library of Medicine, clinical trials can fail for many reasons. Among the top five pain points include problems with (i) patient recruitment; (ii) enrollment; (iii) retention; (iv) safety issues; and (v) failing to maintain protocols or FDA guidance. However, from mitigating FDA audit risks to managing patient recruitment and engagement, there is

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RealTime-eSOURCE: Fueling 28X Revenue Growth at the University of the Sunshine Coast

RealTime-eSOURCE: Fueling 28X Revenue Growth at the University of the Sunshine Coast 

Before partnering with RealTime, UniSC was grappling with huge piles of paper and operational inefficiencies that made it difficult to smoothly conduct multi-site decentralized trials for the rapidly expanding network. Using RealTime’s eSOURCE, they were able to enforce protocol compliance, centralize source documents, eliminate paper workflows and reduce time on administrative tasks with streamlined workflows.

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Streamline eRegulatory (eReg) Document Management with RealTime’s eDocs Solution for Clinical Trials

In the ever-evolving field of clinical research, technological advancements continue to revolutionize how we conduct studies and collect data. One such innovation is the Realtime-eDOCS solution, a game-changer for clinical research sites. In this blog post, we will explore the benefits this eRegulatory (eReg) solution brings to these sites and how it can enhance their

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