ePRO Solutions
invivodata's electronic Patient Reported Outcomes (ePRO) systems drive patient compliance, eliminate recall bias that plague self-report studies and increase the efficiency by which study data is collected. With scientific expertise and knowledge of ePRO best practices, regulatory requirements and patient behavioral sciences, invivodata solutions offer study teams clear advantages. The invivodata solutions, which include DiaryPRO®, a field-based ePRO system, SitePRO® for site-based PRO data collection, and DiaryPRO® Web for reliable PRO data collection via a Web interface, provide immediate access to study data, giving researchers and sponsors visibility into study progress and improving trial efficiencies.
invivodata's solutions are unique in that they:
- Help sponsors to support labeling claims. invivodata's solutions provide sponsors with trust-worthy data that can be used reliably in new drug applications.
- Provide more efficient trial management. Unlike other ePRO solutions on the market that are focused simply on collecting patient data, invivodata's solutions provide proactive patient and site management functionality, reduce the data management requirements of a given study, and are designed to support a quicker database lock.
- Provide flexibility to accommodate study needs. invivodata's solutions help support shorter development timelines, allow for seamless mid-study changes with in-field updates and allow for thoughtful changes which may be required to meet evolving regulatory considerations.
Because there are many factors to consider when selecting an ePRO solution for clinical development programs, invivodata offers scientific and regulatory support as you make critical decisions about ePRO modality options. Contact us today to learn which solution is right for your trial.