Due to the global health impact of COVID-19, many aspects of daily life have been moved to a hybrid model, meaning a mix of in-person and technology-enabled interactions In this blog, learn why eCOAs are especially well-suited for hybrid clinical trials.

Discover why the use of electronic clinical outcome assessments (eCOA) in clinical research is becoming an increasingly important part of study design in this article.

Consider this expedited review approach to facilitate the efficient evaluation of COAs and eCOAs, streamlining the pathway for successful trial execution.

Drawing on evidence from scientific literature, we examine the pitfalls that have hindered its success and propose actionable solutions to unlock its true value in clinical research.

The clinical research industry has been reluctant to adopt eConsent for several reasons. Unearth how the industry should continue exploring and implementing digital technologies in earnest in the future.

Support the digitization of the participant consent process and begin creating multimedia-enhanced electronic informed consent forms (eICFs) that participants sign electronically, eliminating burdensome and error-prone paper-based processes.

See firsthand how this modern build platform, which includes a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.

Explore the importance of involving caregivers in the care process and how electronic patient-reported outcomes technology can facilitate communication, tracking, and collaboration.

We selected and evaluated a non-consumer device, to explore its potential as a reliable tool for home-based ePRO measure administration. Here’s what we learned from this usability testing.