Frequently Asked Questions

Review commonly asked questions about MyVeeva for Clinical Trials.

MyVeeva for Clinical Trials is a patient engagement platform used by clinical research sites to improve efficiency and make it easier for patients to participate in clinical trials. MyVeeva will include capabilities for eConsent, virtual visits, patient adherence, and ePRO.


MyVeeva for Doctors makes it easy for healthcare providers to connect with the life sciences industry. Doctors and staff can search for contacts, companies and brands. They can connect with reps and medical science liaisons and see digital materials and patient resources shared by sales reps and brand teams. MyVeeva for Doctors is integrated to Veeva CRM and is planned for availability in December 2020.


MyVeeva is planned for availability to early adopters in January 2021.


MyVeeva for Clinical Trials will be free for investigative sites.


There is not a limit on the number of studies, users, or participants that you can have in the system.


MyVeeva will be available via desktop or mobile device. Patients will primarily use MyVeeva via an iOS/Android app on their personal smartphone. Sites will access MyVeeva via a website.


The use of SiteVault Free or SiteVault Enterprise is required for access to MyVeeva for Clinical Trials. Sites can sign up for SiteVault Free here.


MyVeeva will integrate seamlessly with Veeva SiteVault.


This content is intended for informational purposes only and does not form part of any contract. It is not a commitment to deliver any specific functionality. Features and functions described in this document will be released commercially only when and if they become available. The development, release, and timing of the features or functionality of Veeva’s products remain at the sole discretion of Veeva.

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