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

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/