What have sites been experiencing in the adoption of eSource?  What’s working well and what presents barriers or burden to sites? What real challenges might influence sites to proceed with caution? This session is designed to help clinical research sites make informed decisions regarding the adoption of eSource systems. Whether you are considering eSource for the first time or seeking ways to optimize its usage, this session will cover key topics like risks and benefits, operational considerations (like SOPs and infrastructure requirements), transition planning for your organization, supplier assessment, and budget considerations.

Learning Objectives:

1. Understand the risks, benefits, and considerations involved in eSource adoption at the site level.
2. Learn effective strategies for developing SOPs, transition planning, and change management during the integration of eSource systems.
3. Gain insights into assessing suppliers, compliance, prioritizing feature adoption, and implications for remote monitoring and remote PI oversight.