eCOA data must be accurate, relevant and understandable; SmartReports delivers all three - and more. SmartReports includes a broad array of over 18 standard reports.
SmartReports is the most powerful tool available for viewing, managing and understanding clinical research trial patient data. Its interactive interface is intuitive and provides an unprecedented level of detail within patient data reports. This enables project managers, monitors and sites to sort by report headers; drill-down within subject and site data; and view reports in native language translations.
SmartReports delivers on the PHT ability to anticipate the evolving reporting needs of the ePRO market. The PHT active dialog with our clients coupled with our unmatched scientific and business expertise enables us to take ePRO solutions to another level.
StudyWorks always sets the standard for completeness of reports offered and usefulness of data in eDiary trials. SmartReports raises the bar on reports for managing compliance, eligibility, and enrollment – all the aspects of successfully integrating ePRO data in clinical trials. Being able to sort on subject and site data saves a lot of time.
SmartReports runs entirely within StudyWorks with no plug-ins or additional software. It enables enrollment, compliance and eligibility reports to be displayed in many different languages. This is particularly useful and advantageous for clinical sites that prefer to view reports in their native language.