Veeva ePRO allows site staff to manage participant and site staff surveys.
Note Veeva ePRO is only available to sites whose sponsors are using Veeva ePRO in Clinical Operations.
If your study’s sponsor uses MyVeeva Studio to create participant and site staff surveys to collect study data, you can use Study Connect to manage your study’s surveys. The Surveys section of Study Connect will help you manage the following survey types:
- Electronic Patient-Reported Outcomes (ePRO): Participant surveys completed in the MyVeeva for Patients application.
- Electronic Clinician-Reported Outcomes (eClinRO): Site Staff surveys completed from SiteVault.
When your study is connected to Veeva ePRO, you can add supported languages for your study, approve survey collections that your study’s sponsor creates, enable participants with ePRO, manage their study events, and complete site staff surveys.
General ePRO Workflow
The process of using Veeva ePRO in Study Connect uses the following general steps:
ePRO Troubleshooting Resources
See the following pages for additional resources about troubleshooting Veeva ePRO in SiteVault and MyVeeva for Patients: