IRT eCOA

IQVIA’s Integrated IRT eCOA Solution

Improve study quality, accelerate decision making and reduce site and sponsor burden by harnessing the power of IQVIA’s integrated Interactive Response Technology (IRT) and electronic Clinical Outcome Assessment (eCOA) solution. Now, with an option to add IQVIA Complete Consent to support patient enrollment and study efficiency.

Orchestration Goals

Integrate best-of-breed solutions, producing a validated platform built for configurability, rapid study start-up and flexible mid-study changes that also:

  • Reduce task timelines and study burden to improve experience for all stakeholders
  • Seamless platform that eliminates redundant, duplicative activities, like data entry and multiple logins
  • Improve data quality and integrity, eliminating the need for data reconciliation
  • Leverage insights from patient data quickly to improve compliance, supply optimization, and decision making
  • Accelerate timelines, streamline change management, and improve overall experience

IRT eCOA orchestration benefits

and the opportunity for human error as clinical teams are relied on to re-enter data in multiple systems.
during the start-up and maintenance phases of the trial through workflow automation and optimization.
Parallel study builds, contrasting integrated and unintegrated solutions, show site process optimization and time savings during study build, delivery and execution.
With one orchestrated system, one point of contact during study design, implementation and management and the option for one UAT. Time to database lock is expedited by eliminating need for data reconciliation.
entries for site activation, patient screening, stratification, randomization, as well as updates to visit scheduling from source systems.

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