We collaborated with relevant product stakeholders, understood their business goals, the primary end-user profiles, and their goals as well as challenges. We leveraged the power of technology to digitise paper-based case report forms, and centralise data from various sources.
This resulted in a significant increase in data reconciliation and reporting efficiency, reduction in patient risks, and costs in conducting trials owing to manual tasks.
- UX Audit
- Task Flow Optimization
- Navigational structure Redesign
- Wireframing
- Visual Design
The Engagement
Summary of main achievments when we started
Centralised & real-time clinical trial data reporting
Real time reporting & centralised data visualization on electronic case report from data
Data transparency and trustworthiness
Consent replaces the paper-based informed consent document. This provides real-time visibility and central tracking of recruitment and enrolment metrics across trial sites.
Digital Forms
End-users can drill-down to review the data and related details for quality checks.
- Reduction in time to data discovery: 33% Reduction
- Saved hours of manual work: 18k+ hrs Saved Source: https://www.copods.co/case-studies/trial-management/
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