Solutions

Keep Clinical Review and Study Responsibilities Visible

Investigators & Study Teams

Investigators and coordinators carry the day-to-day responsibility for study execution. Evoright 360 is being developed to keep clinical review and study responsibilities visible so investigators can focus on oversight while coordinators manage execution, with AI-assisted support that staff review and control.

How Evoright 360 helps

Planned value for investigators & study teams

These are planned capabilities. Availability will be confirmed as the platform is released.

  • Track participants, visits, and milestones in one view
  • Manage tasks and outstanding reviews without losing context
  • Use AI-assisted summaries and task suggestions for daily work
  • Keep source and regulatory records connected to each study
In detail

What connected workflows mean here

Visit preparation

Coordinators see upcoming visits, required procedures, and outstanding preparation tasks. Visit windows and scheduling anchors are configured from the protocol so the team works from approved rules.

Assigned reviews

Investigators see source records and items assigned for their review, with open comments and sign-off requirements. Review responsibilities are configurable per study and role.

Source documentation

Source records are organized around protocol-defined visits. Completeness checks highlight missing entries for review; checks never fabricate values or alter clinical records.

Training and qualifications

CVs, licenses, GCP certificates, and study training are tracked with expiration dates. Investigators and coordinators can see what is current and what needs renewal.

Follow-up and retention

Missed appointments, outstanding contact attempts, and follow-up tasks are visible so the team can engage participants who need additional attention.

Workflow example

How it comes together

A coordinator prepares for a visit while the investigator reviews assigned items. The distinction between investigator oversight and coordinator execution is preserved throughout.

  1. 1

    The coordinator reviews the upcoming visit schedule and required procedures.

  2. 2

    Source documentation is completed using the protocol-defined visit template.

  3. 3

    Completeness checks highlight outstanding entries for the coordinator to resolve.

  4. 4

    The investigator reviews assigned records, opens comments, and signs off.

  5. 5

    Training records and qualifications are confirmed current for the study.

Frequently asked questions

Discuss Your Site's Needs

Let's talk about your site or network

Evoright 360 is in development. Tell us about your workflows and priorities, and our team will walk through how the platform can come together for your site or network.

Evoright 360 does not collect patient information through this form.