VEEVA eConsent

Better Inform Your Patients
with Veeva eConsent

Deliver a better site and patient experience through an
end-to-end informed consent process.

Announced 2021
Status Early

Veeva eConsent provides a digital way to consent clinical trial participants in-person or remotely.

Sponsors manage the consent forms in Vault. They can be authored in Word and digitized to include interactive elements like videos, questions, and signatures. Blinded consent data can also be viewed through the sponsors/CRO vault.

Sites are able to review and update consent documents, view participant consent status, and countersign the consents.

Participants, or other signatories consent via MyVeeva for Patients (native application or web). This is also used to access study documents and complete multiple study activities, including ePRO and visit management.

Why Veeva eConsent

Make participation in clinical trials easier

  • Better patient experience

    Give patients direct and convenient access to their study documents on their own device.
  • Reduce site burden

    Remove administrative burden by using one eConsent system across all studies.
  • Faster study execution

    Accelerate informed consent form (ICF) creation and review by eliminating manual processes.
  • Stronger compliance

    Streamline consent monitoring and stay informed with complete visibility into consent status.


Explore and learn

Celerion enhances patient-centricity and improves efficiency
Read case study
Break down the barriers to eConsent adoption
Read article
Patient-centric eConsent: deployed in days, updated in minutes
Download features brief

Interested in learning more about how Veeva can help?