Copods

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

    TRANSFORM

    1 Designer

    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.

    Structural changes to the product for future proofing.

    Reduction in time to data discovery

    33%
    Reduction

    Saved hours of manual work

    18k+ hrs
    Saved

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