Remarque Systems

Watch Mark’s Story

A comprehensive SaaS application for designing, deploying, and managing clinical trials with a risk-based approach. See how Mark takes control with Remarque Systems.

Assessment Services

Optimize areas prone to human error

  • Workflow assessment

  • Risk mitigation assessment

  • Applications assessment

  • Business Intelligence assessment

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Workflow Platform

Trial protocol Integration

Protocol integrated workflow process and system-maintained audit trail to know you are prepared for Investigator or Central Monitor visits.

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Standards: FDA, ICH, more…

Ingesting Data from Various Sources

Our primary customers are pharmaceutical, biotechnology, medical device and contract research organizations. We understand the importance of being fully compliant with FDA, ICH and other regulatory and industry standards.

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Remarque Systems

Optimize Your Enterprise

Remarque Systems is a leader in innovative clinical research methods. We optimize clinical trials and enable enterprise collaboration.

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Why Choose Remarque Systems?

Inspect what you Expect

  • Increased patient safety

  • Improved data management

  • Optimized clinical operations

  • Shared therapeutic area insights

  • Speed and accuracy pharmacovigilance improvements

Mitigates Risk

  • Prediction

  • Detection

  • Analysis

  • Management

Advanced Data Analysis

  • Machine Learning

  • In-Process Analytics

  • Enhances Data Visualization

Industry Knowledge & Recognition

  • Fully Compliant with FDA, ICH and other regulatory and industry standards

  • “20 most promising QMS solution providers in 2018” by CIOReview Magazine

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Our Platform

Leverage Existing Systems, Don't Replace Them

We don't replace your existing systems, we connect them! Your company has spent years investing in the right software. Don't scrap it to enable cross-departmental optimization. Remarque Systems Platform allows departments to operate the same while enabling real-time, meaningful, insights across impacted departments.

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Our Solutions

Fully Customizable, Growing in Uses

Integrated workflow process and system-maintained audit trails are just the beginning. The entire system is fully customizable. It allows a completely vendor agnostic approach to your data and can ingest from any EDC, CTMS or lab data platform. It is fully compliant with FDA, ICH and other regulatory and industry standards.

Solutions & Services

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