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Robust and compliant clinical trial management system that facilitates:

  • Secure data management
  • Patient recruitment tracking
  • Site management
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Study management and configuration support

Resonance Study Manager ("RSM") is a software platform connected to Patient Center that is used to manage and monitor data specifically for sponsored or collaborative studies. Designed for research, RSM only manages and analyzes data included in IRB approved research studies. Users can share and analyze data from Patient Center after it has been stripped of private health information. RSM facilitates collaboration and study participation in compliance with regulations regarding private health information and study subjects.

Electronic Case Report Form (eCRF) Creation

Configure project or study specific forms (eCRFs) based on a growing library of standard and dynamic forms to facilitate custom data collection.

Conduct Multi-Center Studies

Streamline the coordination, monitoring, and data management of multi-center studies enabling access to a centralized view of anonymized data ensuring compliance and enhancing communication across sites.

Adverse Event Reporting

With support from Resonance Analytics, configure automated safety reporting pipelines to promptly report serious adverse events (SAEs), adhere to established timelines, and ensure patient safety.

Analytic Pipeline Creation and Management

Create automated analytic pipelines that clean, transform, summarize, and report on study data in a compliant manner based on specific study parameters.