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Uncategorized: Intelligent Monitoring in Clinical Trials

One of today’s big conversations in clinical research is how the conventional approach for monitoring trial conduct simply doesn’t give the best view of data to protect patient safety, comply with protocol procedures and ensure the accuracy of data collected during the conduct of a study. This conventional approach, involving periodic site visits with 100% SDV, is reactive, resource intensive and based on the retrospective detection of errors. ArisGlobal invites you to learn about the value of intelligent monitoring by downloading a complimentary white paper, “Intelligent Monitoring in Clinical Trials.” This paper describes the various types of risks involved and the importance of a framework that combines optimal monitoring strategies to support decisions about the type, intensity and frequency of monitoring a site during clinical trial conduct. [contact-form-7 id="41" title="download the White Paper Default"]
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