Electronic Clinical Outcome Assessments (eCOA)

Giving you tools to listen.

When collecting information, reported data can be a powerful, and deeply personal, tool. Whether in regards to a volunteer’s symptoms, mental wellbeing, or side effects, electronic clinical outcome assessments (eCOAs) can give a considered picture of if and how an investigational treatment is functioning.

Some COA measures include:

  • Patient-reported outcome (PRO)
  • Clinician-reported outcome (ClinRO)
  • Observer-reported outcome (ObsRO)
  • Performance outcome (PerfO)

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Our extensive work with eCOA studies and commitment to supporting everyone who uses our technology means a full suite of capabilities, including:

  • Scientific consulting to help generate relevant, valid, and high-quality data for smooth submission to regulators, payers, and other market access stakeholders
  • Knowledgeable project oversight and communication on project plans, risk management, and issue management for your study needs
  • Comprehensive study delivery services including 24-hour helpdesk, telecoms support, and data transfers
  • Logistics to ensure equipment arrives at sites in time, all supported by our extensive network of regional hubs and in-country depots, and by our decades of navigating customs regulations
  • eCOA technology Clinical Ink's SureSource platform provides trial sponsors, investigators, and volunteers the real-time visibility they need to help improve adherence to protocol execution, reduce trial risk, and improve patient safety and engagement
  • Patient wearables and sensors integrate with the expanding realm of devices to collect biometric data

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We are always available for a conversation.

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