Accelerating study start up through an eCOA library
This insight brief details how IQVIA's new global library of pre-built assessments provides robust electronic measures on-demand, giving sponsors instant access to validated, purpose-built tools that capture the patient's perspective in a given study.
White Paper
Nov 06, 2019


As the pharmaceutical industry continues to move towards a more comprehensive picture of treatment benefits for new drugs in development, patient reported outcomes have become a new benchmark for regulators and payers to measure the quality of a drug or therapy. This shift has made Clinical Outcome Assessments (COA) an increasingly necessary and often required tool in the clinical research landscape.

COAs offer a direct line to the patients, capturing insights about their experience with their disease, the trial, and its impact on their quality of life. And now electronic COAs, or eCOA, are enabling this in real-time. These insights give patients a chance to be heard while providing sponsors with patient-relevant endpoints to better understand the impact and efficacy of a treatment. Capturing insights directly from patients helps researchers design trials around their needs, while increasing the likelihood of drug approval and reimbursement.

However, creating and validating a COA in an electronic format adds months to the trial planning process. Sponsors can spend 12-16 weeks at a minimum building an assessment in an eCOA system, validating it against standards, qualifying it with relevant approvers, and adjusting/translating the tool as necessary. In many cases, revision and approval delays cause this planning step to extend well beyond the deadline, delaying firstpatient-in milestones, which can drag the entire schedule off track. This adds time and cost to the trial. It also increases the risk that the questions they ask will vary from assessment-to-assessment, making it more difficult to compare results across trials or patient populations.

Historically, sponsors have repeatedly re-created standard eCOAs for every trial, but what if they didn’t have to? The industry has enough experience in eCOA development and validation that sponsors could leverage existing assessments in new trials with minimal or no modifications. 

To fill this need, IQVIA has created a standardized library of assessments with more than 500 eCOAs that have been pre-built for use in a range of trials to meet patientreported outcome goals. The library is a one-stop-shop for eCOA tools, which sponsors can instantly deploy as part of their trial process. This collection of industry validated assets promises to accelerate trial delivery while ensuring every assessment captures the right data at the right time. 


Download to Read More
Related Solutions
Clinical Trials

Change the model of clinical research by integrating data, expertise, analytics and technology from study design through execution to power better decisions.

You may also be interested in
Contact Us
Contact Us
Contact Us

Email Us

Get in touch today to discover the right solutions for you.

Call Us

We are pleased to speak with you during our standard business hours.

U.S. Toll-Free only
+1 866 267 4479

For international call please find a number in our toll-free list.