Configurable alarms appear as banner alerts on subjects’ devices, while email notifications help sites monitor potential non-compliance and respond to newly uploaded symptom severity data.

Electronic Clinical Outcome Assessment (eCOA) has transformed data collection in clinical trials by prioritizing patient engagement and improving data accuracy.

Learn how researchers were able to effectively collect payments, drive engagements, and present value to the sponsor, sites, and patients.

Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.

In part one of this series, the author dives into how electronic consent platforms are simplifying and improving the trial experience for patients and sites.

Scott Askin paints the picture of why Novartis, determined to improve the patient experience, has begun to deploy eConsent, and what they’ve learned along the way.

What makes a clinical trials software provider a good fit? How do you make the decision to use a particular electronic data capture (EDC) system or electronic patient reported outcome (ePRO) solution? Learn how the answers are different for every sponsor and contract research organization (CRO).

Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.

Industry experts discuss how a medical device company implemented ePRO to close gaps in data accuracy, reduce context switching for staff, and enhance patient convenience.