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ABSTRACT: Background
Data standards are not only key to making data processing efficient but also fundamental to ensuring data interoperability. When clinical trial data are structured according to international standards, they become significantly easier to analyze, reducing the efforts required for data cleaning, preprocessing, and secondary use. A common language and a shared set of expectations facilitate interoperability between systems and devices.Objective
The main objectives of this study were to identify commonalities and differences in clinical trial metadata, protocols, and data collection systems/items within the VACCELERATE project.Methods
To assess the degree of interoperability achieved in the project and suggest methodological improvements, interoperable point
SUBMITTER: Malik S
PROVIDER: S-EPMC11928774 | biostudies-literature | 2025 Mar
REPOSITORIES: biostudies-literature