APIs in Clinical Trials Explained: What They Are and Why Your Site Needs One
July 16, 2025
Clinical trial sites and site networks often rely on a growing stack of tools. Many sites now run critical workflows
Do You Need to Validate Your CTMS After Every Update? Here’s What Research Sites Should Know
July 10, 2025
When it comes to compliance, one question keeps popping up for clinical research sites using electronic systems: “Do we need
How to Accelerate Study Start-up in Clinical Trials: From Feasibility to First Patient In
July 8, 2025
Despite experienced teams and best intentions, many research networks find themselves stuck in the same cycle: late feasibility responses, fragmented
Transitioning from NIH-Funded to Pharmaceutical-Funded Trials: Leveraging Performance Metrics and Expertise
July 2, 2025
The funding landscape for clinical trials is undergoing a significant transformation. As grant support for NIH-funded studies continues to decline,
How to Prepare for an FDA Audit: A Comprehensive Guide for Clinical Research Sites
June 18, 2025
When the FDA announces an audit of your clinical research site, it can feel daunting. However, with proper preparation, your
How to Measure the ROI of eSource: A Real-World Framework
June 11, 2025
Clinical research sites are constantly balancing time, quality, and cost, often with limited resources and increasing complexity. “How to Measure
Webinar Recap: Best in Breed vs All-in-One – The Single eClinical System Advantage
May 27, 2025
Watch the webinar replay here. In a recent webinar, “Best in Breed vs All -in-One – The Single eClinical System
How to Build Better eSource: A Masterclass with Shantell Gomez
May 22, 2025
About Shantell Gomez, eSource Build Specialist: Shantell Gomez is an experienced eSource Build Specialist with a background as a Clinical