Getting Started with ePRO/eCOA

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The benefits of electronically collecting data directly from clinical trial participants are well documented, and include higher-quality data, reduced data management and monitoring effort, and increased patient engagement. However, many researchers have yet to make the transition from paper to electronic in this area. This webinar is designed to help researchers bridge this gap and develop a successful eCOA strategy by looking at available technology, regulatory requirements, and procedural changes that commonly come with this transition. 

Please fill out the form to download our webinar "Getting Started with ePRO/eCOA".