Adopting eSource capabilities reduces the time, human resources and errors typically associated with transposing clinical trial data from paper-based forms or disparate systems. Efficiencies can be gained across teams, from clinical operations to data management. However, implementation of such systems is often easier said than done. Innovative solutions designed with interoperability across multiple systems remove the technological barriers for easier, faster, cheaper integration of data sources and existing eClinical systems. In addition, flexible integration solutions allow new sources to be added as they continue to proliferate.
Using examples from site-based devices and information sources, representatives from Bioclinica and Adaptive Clinical will discuss the data and workflow benefits of integrating participant data (from site-based devices and electronic health records) directly into eClinical systems, such as EDC and CTMS. They will also discuss the importance of interoperability for reduced implementation times and share the data management and clinical operations efficiencies gained from real-time access to quality data.
What you will learn: