Automating clinical research data, and trial management
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

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