MyVeeva for Patients

Overview

MyVeeva for Patients is designed to simplify and improve the clinical trial experience for participants by centralizing all necessary information and resources. It allows patients to manage trial-related activities through an intuitive interface.

Participants can easily access important information including trial documents, additional resources, and contact details. The study homepage provides a comprehensive view, streamlining the information retrieval process.

To help participants manage appointments, the platform provides details on upcoming study visits, including direct access links to virtual visits, ensuring clarity on the logistics of their participation.

The platform also supports patients who need non-urgent assistance. Users can flag queries and request support directly through the system, eliminating the need for direct phone calls to clinical sites.

Another key feature is eConsent capability which allows patients to review and complete informed consent documents online. This feature incorporates interactive elements like videos and questions to guide patients through the consent process effectively.

MyVeeva for Patients also simplifies the completion of ePROs, providing timely notifications and enabling forms completion through a user-friendly web platform or mobile app.

• Centralized access to study documents and resources
• Management of in-person and virtual appointments
• Direct support request feature
• Online informed consent with interactive elements
• User-friendly electronic patient-reported outcomes submission