Efficiency & Quality: The Impact Of CDASH eCRFS On Clinical Trials

Clinical trials are continually evolving to become more efficient and precise, and one of the most significant advancements in this domain is the adoption of CDASH (Clinical Data Acquisition Standards Harmonization) eCRFs (electronic Case Report Forms). In this article, we explore the dissemination of CDASH eCRFs via the CDISC eCRF Portal and the OpenClinica Electronic Data Capture system.
Published in the Journal of the Society for Clinical Data Management (JSCDM), our article has garnered over 1,100 views and 270 downloads within a year, reflecting the keen interest of clinical trial professionals in leveraging validated CRF content. The implementation of CDASH eCRFs promises numerous benefits, including improved efficiency for study designers, greater adoption of high-quality standards, reduced delays, fewer protocol amendments, faster implementations, lower start-up costs, and enhanced data reusability.
Join us as we delve into the transformative impact of CDASH eCRFs on clinical trials and their potential to revolutionize the field.
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