Learn about help, release, and known issue resources for MyVeeva for Patients and the Veeva Digital Trials Platform products that integrate with it.
Note Veeva eConsent may be provided by your sponsor for use on a Connected Study or enabled for your SiteVault account as a paid add-on to use across all studies. Contact the Site Success Team to learn more.
Note Veeva ePRO is only available to sites whose sponsors are using Veeva ePRO in Clinical Operations.
The following resources are available for MyVeeva for Patients, Veeva eConsent, and Veeva ePRO:
| User |
Resource |
Description |
| MyVeeva for Patients User |
Help |
The MyVeeva for Patients Help website documents how to complete tasks as a MyVeeva for Patients user, for example, how to register an account, complete eConsent forms, and take ePROs (surveys).
|
| MyVeeva for Patients User |
Release Notes |
The MyVeeva for Patients Release Notes document the features and issue corrections in releases from a MyVeeva for Patient's point of view.
|
| Site Staff |
Help |
The following resources are available for Veeva eConsent:
- SiteVault eRegulatory Help: The SiteVault eRegulatory Veeva eConsent help beginning on the Overview of Veeva eConsent page documents how to author eConsent forms and consent participants electronically in eReg.
- Study Connect Help: The Study Connect Veeva eConsent help beginning on the Overview of Veeva eConsent page documents how to manage eConsent forms and consent participants electronically in Study Connect.
- Veeva eConsent Editor Help: The Veeva eConsent Editor Help documents how site and sponsor staff can use the editor to transform source documents into eConsent forms.
The following resources are available for Veeva ePRO:
- SiteVault eRegulatory Help: The Veeva ePRO help beginning on the Overview of Veeva ePRO page documents how to connect your study to your sponsor’s ePRO collection, enable study participants with ePRO, manage ePRO collection documents, and export ePRO-related data in eReg.
- Study Connect Help: The Veeva ePRO help beginning on the Overview of Veeva ePRO page documents how to connect your study to your sponsor’s ePRO collection, enable study participants with ePRO, manage ePRO collection documents, and export ePRO-related data in Study Connect.
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| Site Staff |
Training |
The SiteVault Training Resources page provides Veeva eConsent training resources. On the page, you can register for a group training session about how to use Veeva eConsent and MyVeeva for Patients to consent participants electronically.
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| Site Staff |
Troubleshooting |
See the following resources for information about how to troubleshoot during the Veeva eConsent authoring and consenting processes or while using Veeva ePRO in SiteVault:
- Veeva eConsent:
- Veeva ePRO:
|
| Sponsor Staff and Site Staff |
Release Notes |
The resources below are available across the Veeva Digital Trials Platform. We recommend that you visit whichever release notes apply to you to understand everything that is included in a general release.
- Digital Trials Platform: The Digital Trials Platform release notes document general releases and impact assessments for MyVeeva for Patients, SiteVault, Site Connect, Veeva eConsent, and Veeva ePRO.
- SiteVault: The SiteVault Release Notes document what's new for sites.
- Site Connect and Vault Clinical Operations: The Vault Release Notes document Vault releases and impact assessments, which include descriptions of new Site Connect and Clinical Operations features.
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| Site Staff |
Known Issues |
The MyVeeva for Patients Known Issues page documents known issues that affect users of MyVeeva for Patients, the Veeva eConsent editor, and the Veeva ePRO module.
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