A large pharmaceutical company conducting an early Phase I study was looking for an electronic data capture solution that would offer real-time access to study data, eliminate manual data re-entry, minimize data errors and facilitate the remote monitoring of research sites. The sponsor worked with Clinical Ink to develop a customized eSource study to capture data electronically during the subject visit. Learn more about this company’s experience in a free case study.
What you’ll find in this case study:
- How Clinical Ink’s eSource platform delivered and validated data within minutes of a subject’s visit
- How a custom study improved the ability to remotely monitor and analyze safety data
- How Capture reduced site workload, timelines and costs and satisfied site users