Research Grid’s Metrics & Reporting solution enables trial teams to track engagement, extract meaningful insights, and create tailored reports that support study delivery, operational oversight, and regulatory documentation. Design surveys, collect study data, and generate custom dashboards with precision and speed.
End-to-End Data Collection and Visibility
Whether you're tracking participant engagement, assessing site performance, or monitoring protocol compliance, Research Grid centralizes your metrics in one platform. Combine real-time data collection with automated reporting to streamline trial operations and accelerate decision-making.
Collect the right data with tools designed for clinical workflows across stakeholders, trials, and geographies.
Create customized surveys and assessments with branching logic, color coding, and multilingual options.
Value for Clinical Trial Stakeholders
Sponsors
Track study performance and participant engagement in real time.
Access accurate, centralized data for oversight, risk mitigation, and reporting across all programs and geographies.
CROs
Simplify operational reporting and reduce manual reconciliation.
Monitor trial delivery metrics, site activity, and compliance status across studies using customizable dashboards and reporting templates.
Sites & Coordinators
Collect feedback and report outcomes with less admin work.
Use simple survey tools to assess participants or staff, submit data instantly, and generate reports without relying on external systems.
Features to fit your study needs
Survey & Questionnaire Builder
Create custom surveys with logic, formatting, and visual styling
Use conditional paths and multilingual options for tailored experiences
Build for patients, sites, or internal staff reporting
Real-Time Data Capture & Dashboards
Data Export & Report Generation
AI-Powered Quick Extract
Turn Study Data Into Operational Insight
Gain full visibility into participant activity, site performance, and study health. Use Research Grid’s Metrics & Reporting tools to collect, analyze, and act on trial data with confidence and control.
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