A Suite of Four Core Components
Built to evolve
Entirely customizable, our platform aggregates data from your current systems. This allows our clients to easily manage legacy data and have more compatibility with trial-site systems. The possibilities are beyond imagination: any EDC system, CTMS system, Electronic Health Records, wearable devices and more. All while maintaining full FDA, ICH and other regulatory and industry standards.
A versatile platform to improve clinical subject safety
A comprehensive SaaS application for designing, deploying, and managing clinical trials with a risk-based approach. Integrated workflow process and system-maintained audit trails allow you to take action from within the Remarque Systems interface.
Uncover the hidden story in your data
Any data captured can be used to create a custom DATAPOINT within the system. Once a DATAPOINT is created it can be used in Workflows, Site scoring, and more. These benefits are only possible with the in-process analytics, and machine learning for effective risk prediction, detection, analysis, and management.
Must be continuous within clinical trials
Implement your risk-based monitoring strategy effectively and efficiently, have your teams embrace the process and contribute to its success while being confident that your strategy has the key components it needs to meet regulatory expectations