Consolidated Data.
Identified Risk.
Informed Action.

Remarque Systems brings process optimization, increased visibility, rapid communications, and improved quality to your clinical trial data and operations.

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Consolidate

Seamlessly import data from all disconnected repositories into one single platform. Immediately gain better visibility and oversight so you can take more informed actions.

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Identify

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

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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 Systems to gain better clinical trial data insights.

CASE STUDY

94%
94% less time spent generating clinical trial metrics
100%
100% increase in data visualizations of site-level metrics over time
98%
98% implementation success rate within 3 months
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Our Solution

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

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Our Platform

Vendor-neutral data aggregation. Enhance transparency, accuracy, and efficiency with end-to-end visibility and clear, conclusive analytics and reports in real-time.

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Our Promise

Remarque Systems adapts to ever-changing clinical trial data and regulatory demands — helping you optimize your process along the way.