Clinical Data Management
Veeva eConsent
Daksh Technologies offers Veeva eConsent, a digital solution for consenting clinical trial participants, whether in-person or remotely. Sponsors can manage consent forms through the Vault system, creating them in Word and enhancing them with interactive features like videos, questions, and e-signatures. Blinded consent data can also be accessed through the sponsor/CRO Vault.
Clinical sites can easily review, update, and track participant consent documents, as well as countersign the forms when needed.
Participants, or other signatories, use MyVeeva for Patients (either via the native app or web) to provide consent, access study documents, and complete other study-related tasks such as ePRO and visit management.
Years of Experiences
Best Awarded Company
We adapt our delivery to the way your work, whether as an external provider.
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