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eCOA consortium

Answering the Sustainability Call: Digital Health Technologies and eCOA

With over 350,000 registered clinical trials worldwide, the research industry contributes an estimated 27.5 million tons of CO₂ equivalent, highlighting its substantial environmental impact. Digital health technologies (DHTs) and electronic...

Data Collection in Clinical Trials with Multiple Caregivers

In clinical trials, especially those involving participants unable to self-report—such as children or individuals with cognitive impairments—caregiver-reported data is essential....

Addressing challenges with eCOA at the site-level

The eCOA: Getting Better Together Initiative launched by the Critical Path Institute in 2019 aimed to identify and address issues...

Flexible approaches to eCOA administration in clinical trials: The site perspective

To address the need to embed flexibility in eCOA use, the “Support Flexible Approaches to PRO Data Collection” project was...

Kayentis extends its contribution to scientific research in clinical trial endpoint assessment and joins the Critical Path Institute’s ePRO Consortium

Kayentis announces that it has joined the C-Path's ePRO Consortium, a nonprofit organization dedicated to advance the science of clinical...