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How to Make eConsent Accessible Across Diverse Populations
Designing Accessible eConsent for Inclusive Clinical Trials Making eConsent accessible across diverse clinical trial populations means designing consent flows that…
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When to Use Wearables in a Clinical Trial and How to Get Started
Wearables have moved well beyond pilot projects and proof-of-concept studies. Many sponsors are already exploring how continuous activity, physiological, and…
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How AI Activates the Full Potential of Wearables in Clinical Research
Wearables are no longer experimental. Smartwatches, activity trackers, connected scales, and mobile health apps are already part of daily life…
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What Is ePRO?
Electronic patient-reported outcomes (ePROs) are increasingly important in modern clinical trials. ePRO can record how patients feel, function, and respond…
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What Is eCOA?
Electronic clinical outcome assessment (eCOA) is a way to collect clinical trial data using digital tools. As clinical trials become…
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AI Implementation Challenges with Legacy EDC Systems: Is Your EDC Limiting the Impact of AI on Your Data?
AI is increasingly being adopted in clinical trials to help teams keep pace with growing data demands. The goal is…
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AI in Clinical Trials: Practical Use Cases for Data Management
AI in clinical trials is increasingly being judged by how well it supports real data management work. Instead of focusing…
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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…
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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…
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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…
