Streamlined Access to Study Information
Veeva Vault offers a comprehensive solution to enhance patient experience in clinical trial participation. With MyVeeva for Patients, individuals have a single point of access for all study documents, actions, and communications. This streamlined approach ensures that patients can easily view study information, understand important details, and stay connected with their clinical site.
Empowering Study Participants
MyVeeva for Patients empowers study participants by providing them with essential tools to manage their clinical trial journey. Participants can access vital information, such as trial documents, additional resources, and contact details, directly from the study homepage. This convenient feature enables individuals to stay informed and engaged throughout the entire process.
Effortless Appointment Management
Through Veeva Vault, patients can effortlessly manage their study appointments with ease. They can stay up-to-date on their upcoming visits, including details on when, where, and how the appointments will take place. Additionally, participants can link to virtual visits directly from the app, offering flexibility and convenience in their trial participation.
Seamless Support Request
Veeva Vault simplifies the process of seeking support during clinical trials. Participants can flag any questions or concerns they may have and request non-urgent assistance without the need to call the site directly. This seamless support request system ensures that patients feel supported and cared for throughout their trial experience.
Interactive eConsent Completion
One of the key features of Veeva Vault is the interactive eConsent process. Study participants can review and complete their informed consent using easy-to-follow sections and interactive elements like videos and questions. This interactive approach enhances understanding and engagement, ultimately improving the overall consent process.
Efficient ePRO Completion
With Veeva Vault, participants receive notifications for upcoming ePRO surveys and can complete them effortlessly using a modern experience on the web or through a native app. This efficient ePRO completion process simplifies survey participation, making it easier for patients to provide essential data during their clinical trial.
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