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How EDC-Based SAE Reporting Reduces Time to Detection and Response in Clinical Trials
Serious adverse events (SAEs) are among the most critical data points collected during a clinical trial. The timeliness and accuracy…
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Modern Post-Market Trials Will Be Driven by RWD – Is Your EDC Ready?
The Post-Market Shift: From Sites to Data Streams Phase IV trials used to mean tracking long-term outcomes by continuing to…
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Smarter Clinical Trials for CNS and Pain: AI Analytics and Objective Measurement Tools
Clinical trials in pain and neurological research have historically faced steep hurdles: lengthy timelines, high costs, and subjective data endpoints…
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Ensuring Regulatory Compliance When Using Wearables in Clinical Trials
Regulatory Risks of Wearables in Clinical Trials Are Real (and Avoidable) Wearables have become indispensable in modern clinical trials, tracking…
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The Future of Remote Patient Monitoring in Decentralized Clinical Trials
The Evolution of Remote Patient Monitoring in Clinical Trials Remote patient monitoring (RPM) has come a long way from the…
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How Wearable Devices Improve Patient Engagement in Clinical Trials
Why Wearable Tech Is Changing Clinical Trials Wearable devices are doing more than counting steps—they’re redefining how clinical trials are…
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Bring Your Own Device (BYOD) Clinical Trials: How They Transform Decentralized Data Capture
What Is BYOD in Clinical Trials? Bring Your Own Device (BYOD) is changing the way clinical trials collect and manage…
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The Future of Wearable Technology in Clinical Trials
What Are Wearables and How Are They Used in Clinical Trials? Wearable technology is transforming clinical trials by making it…
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How EDC Software Minimizes Bias in Clinical Trials
The Impact of Bias on Clinical Trials and Patient Safety Bias, despite best efforts and best intentions, continues to impact…
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How EDC Software Improves Patient Safety
The Link Between EDC and Patient Safety The shared commitment among researchers and healthcare providers to patient safety influences every…
