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.
This page answers questions that you may have as you begin using Veeva eConsent. If a participant or signatory is having an issue while using MyVeeva for Patients, see Troubleshooting Veeva eConsent and MyVeeva for Patients. If you’re having an issue editing an eConsent form in the Veeva eConsent editor, see the Troubleshooting the Veeva eConsent Editor section in Clinical Operations Help.
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How do I create an eConsent form?
See the Creating eConsent Forms page to learn how to create and edit eConsent forms.
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How do I create a patient to start the eConsent process?
The process for creating patients to start the eConsent process uses the following general steps:
- Create a study participant.
- Associate a patient profile with the study participant. Ensure that you include a complete email address and a phone number that can receive SMS text messages for the patient.
See also the Prerequisites section in the help for consenting participants for more information