-
Clinical Data Modernization: A 2026 Starter Guide
Clinical data modernization is one of those phrases that shows up everywhere and means something different to almost everyone. In…
-
What Clinical Teams Should Prepare for in 2026: AI, Automation, and Unified Platforms
As clinical trial operations approach 2026, the conversation around technology is shifting. Tools that were once framed as innovative or…
-
Integrating eConsent with EDC: Streamlined Workflows for Seamless Trials
In clinical research, managing multiple digital systems can create unnecessary friction. When electronic informed consent (eConsent) and electronic data capture…
-
Virtual eConsent in Decentralized Clinical Trials: Best Practices and Innovations
Clinical research is increasingly shifting from traditional, site-based studies to decentralized and hybrid models that meet participants where they are….
-
How Contract Research Organizations (CROs) Can Optimize Their Workflows
Clinical trials are becoming more complex, more distributed, and more data-heavy. For contract research organizations (CROs), that means greater operational…
-
Customizing EDC Workflows for Specialty Pharma and Rare Disease Trials
Why Rare Disease and Specialty Pharma Trials Need Custom Workflows Rare disease and specialty pharma trials operate under very different…
-
The Role of EDC in Real-Time Decision-Making During Adaptive Trials
Adaptive clinical trials are built to respond to evidence as it emerges, allowing researchers to make changes midstream without compromising…
-
Why Scalable EDC Systems Matter in Global Pharmaceutical Trials
Clinical development rarely moves in a straight line. Programs expand across countries, add cohorts, refine eligibility criteria, and shift timelines…
-
How EDC Powers End-to-End Data Management in Pharma-Sponsored Clinical Trials
Electronic data capture, or EDC, continues to be a constant in modern clinical research studies. For pharmaceutical sponsors running complex,…
-
How to Improve Patient Outcomes Using eSource Software in Clinical Trials
In the modern clinical research environment, improving patient outcomes is both a regulatory imperative and an ethical priority. The tools…
