The FDA’s 2013 guidance for electronic source data capture promotes the use of eSource in clinical trials to streamline investigations while improving the reliability, quality, ...
Meet research coordinator Anne-Helene Boivin of Centre Hospitalier de Mont de Marsan in France as she shares a quick look into the clinical trial workflow at her research site, ...
Within the FDA’s guidance document issued in August 2023: Postmarketing Approaches to Obtain Data on Populations Underrepresented in Clinical Trials for Drugs and Biological ...
Clinical trial protocol development and maintenance are some of the most critical steps in the lifecycle of a research study. One of the most common (and important) maintenance ...
Patient slot allocation can be a critical element of early phase clinical trials. There may be a limited number of spots in the trial for participants, and the process of enrolling ...
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