During clinical trials, sponsors and CROs provide research sites with Informed Consent Form (ICF) templates. The Veeva eConsent editor allows you to transform source documents such as Microsoft Word informed consent forms (ICFs) into electronic consent (eConsent) forms. You can create, edit, and save eConsent forms in your Clinical Operations Vault.
In Clinical Operations Vaults with Veeva eConsent enabled, you can exchange eConsent forms with study sites. Study sites can then use the templates to create ICF documents and distribute the approved eConsent forms to study participants. Study participants sign these forms in MyVeeva for Patients.
For sponsors, Veeva eConsent is available if you license and configure it. For sites, Veeva eConsent is a free feature in SiteVault.
Contact Veeva Support to add Veeva eConsent to your Clinical Operations Vault.
Related Articles
Learn about using Veeva eConsent in these articles:
- Veeva eConsent Authoring (Clinical Operations)
- Overview of Editing eConsent Forms
- Importing an eConsent Form
- Creating, Viewing, and Editing an Econsent Form
- Setting the eConsent Form Settings
- Working With eConsent Sections and Content Blocks
- Saving and Checking in an eConsent Form
- Previewing, Downloading, Sending, and Exchanging an eConsent Form
- Troubleshooting the Veeva eConsent Editor
Admin Articles
Learn about configuring Veeva eConsent in these articles: