Choose the Best COA for Your Clinical Trial

With the Clinical ink platform, make data collection and analysis easier: realize improved clinical trial efficiency, quality, and safety, have real-time data access and review, and eliminate data errors.

Choose the Best COA for Your Clinical Trial

Determining which Clinical Outcome Assessments (COAs) or Electronic Clinical Outcome Assessments (eCOAs) are best suited for your study can be confusing, leading to study delays. With the Clinical ink platform, make data collection and analysis easier: realize improved clinical trial efficiency, quality, and safety, have real-time data access and review, and eliminate data errors often seen with other data capture methods.

The Complexities of Clinical Outcome Assessments

Clinical Outcome Assessments are the foundation for proving the effect of an intervention which supports endpoint success for approval. Unlike biomarkers that rely completely on an automated process or algorithm, COAs depend on the implementation, interpretation, and reporting from a patient, a clinician, or an observer.

The study indication, complexity, patient criteria and endpoints each impact leveraging the power of the four types of COAs, which are:

  • Patient-reported outcome (ePRO)
  • Clinician-reported outcome (ClinRO)
  • Observer-reported outcome (ObsRO)
  • Performance outcome (PerfRO)

The Advantages of the Clinical ink Platform

Remotely configure electronic assessments and capabilities for real-time patient monitoring and improved data quality

Manage patient security and privacy with a unique patient-created PIN that also means all questionnaires submitted include a full audit trail, with PIN authentication detail
Manage patient security and privacy with a unique patient-created PIN that also means all questionnaires submitted include a full audit trail, with PIN authentication detail
Provide modules for patient health observations and other aspects
  • By fostering collaboration between patients and investigators, improve the patient experience
  • Implement personalized text message reminders and tasks to improve protocol compliance and adherence
  • Provide appointment and scheduling directly on patients’ personal smartphone calendars
  • Engage patients with study-specific content, educational materials, and on-device training
  • Provide patients with personalized study progress and status in real-time
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