Consolidated Data. Identified Risk. Informed Action.

By bringing all your trial data together in one location Remarque® supports process optimization, increased visibility, and improved quality to your clinical trial data and operations.

A quick summary of site-level data including site demographics, a drill down to patients within the site, and access to data that offers insight based on prior KPI thresholds.

A quick drill down to patient-level data to determine which patients are outside of threshold values, allowing easy creation of workflows for escalation and assignment of follow-through to resolution.

Consolidate

Seamlessly bring your data together from disparate systems into a single location to gain better visibility and oversight so you can take informed actions.

Identify

Quickly identify known and unknown risks with trial-specific triggers — data outliers, adverse events, enrollment issues — in real-time. Better manage risks with greater oversight, collaboration, and visibility.

Inform

Get real-time oversight and end-to-end visibility over all your clinical trial data. Streamline your operations with clear, conclusive analytics and reports based on AI-powered data-driven insights.

The Result

All clinical trial data flows through one powerful platform — empowering increased visibility, better insights, and more informed actions.

Organizations around the world use Remarque® to gain better clinical trial data insights.

94%

94% less time spent generating clinical trial metrics

100%

100% increase in automated data visualizations of site metrics

98%

98% implementation success rate within 3 months of project initiations

Our Solution

Consolidating all clinical trial data under one powerful platform delivers higher quality data, deeper insights, and clear decision paths.

Our Platform

Vendor neutral data aggregation with no coding required. Fully supports next generation trials including DCT’s and is designed to create and maintain historical knowledge.

Our Promise

Remarque® fits into any ecosystem supporting any type of trial. We adapt to changing clinical trial design, changing types of data, evolving regulatory demands – helping you optimize your process and minimize risk along the way.

Case Study

Our strategy enabled the client to identify specific patients at risk of discontinuation—and information on why each of those patients is at risk. Our client was then able to engage in targeted activities to optimize retention.

Case Study

By centralizing the data on the Remarque platform then applying an RBM strategy, the CRO streamlined SDV while swiftly identifying anomalies. The CRO was able to roll out the analytics plan to their study team—and ultimately, to the sponsor. Ultimately, they could save time, reduce costs, and minimize risk both for the sponsor and for the patients.

Case Study

“A nimble company with a focus on customer service, Remarque spent the time to brainstorm various configurations to find the optimal solution for their client, then was able to offer end-to-end deployment that noticeably abbreviated the implementation timeline. In short: They were able to launch the study in record time, while maintaining the safety of the trial team.”

Case Study

“We knew that implementing Remarque technology would improve our efficiency, but it was impossible to understand how dramatically our efficiency would increase until we actually implemented the technology and experienced the difference. We now do in 30 minutes what used to take a full 8-hour day.”

Let’s Talk

Learn how you can transform your clinical trials with Remarque®.