Academic Medical Centers (AMCs) and health systems often rely on Microsoft SharePoint as a document management solution for clinical trials.
The FDA’s recently released draft guidance, “Considerations for the Use of Artificial Intelligence to Support Regulatory Decision-Making for Drug and
In clinical research, electronic source (eSource) systems are transforming how data is collected, managed, and utilized. However, as with any
In 2025, clinical research will continue to undergo significant transformation driven by key initiatives and updates from regulatory authorities like
2025 is set to bring new advancements in clinical trial site management driven by technology, efficiency demands, and industry growth.
Sponsors are raising their expectations for clinical research sites to deliver higher levels of efficiency, data integrity, compliance, and patient
At the recent Decentralized Trials & Research Alliance (DTRA) conference, industry leaders took to the center stage to discuss one
Electronic Source (eSource) presents a compelling case for reducing monitoring costs in clinical trials. By streamlining data collection, improving accuracy,
RealTime eClinical Solutions is a leading, enterprise-grade technology provider facilitating global clinical trials with a comprehensive eClinical platform. Purpose-built for clinical research sites, site networks, academic medical centers, sponsors, and CROs, the platform goes beyond traditional CTMS to empower research and business workflows for modern-day clinical trials.
