In this article, learn more about COAs, and their electronic counterparts, eCOAs.

Explore an eClinical platform with a native mobile app for seamless data capture and study management, featuring advanced AI capabilities that deliver powerful analytics and reporting.

Hear how Medable worked with a Japanese sponsor to elevate their trial experience, achieve >90% patient and site adherence, and beat their forecasted FPI date, creating new eCOA standards adopted across all the customer’s vendors.

This on‑demand session offers a clear, practical overview of the major eSignature types used in eConsent — ranging from simple electronic signatures to fully qualified electronic signatures — and explains when each is appropriate.

Despite the challenges associated with large volumes of data, maintaining quality and regulatory compliance, and enhancing patient engagement, the solutions for managing them can be simple and efficient.

Learn about some insights that have been gleaned from experience deploying eConsent on diverse trial types around the world.

Optimize flexible electronic patient-reported outcomes that allow participants to switch between site-owned devices, personal hardware, and remote completion.

Electronic modes have been shown to improve data quality in clinical trials. Address how equivalency can be achieved when migrating PROs from paper to ePRO.

Download the available infographic to discover how collecting ePRO & eObsRO data via interview mode can be recommended in specific circumstances.