Datasheet | June 24, 2024

Veeva eConsent Features Brief

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Veeva eConsent streamlines the setup, completion, and review of consent processes, significantly reducing administrative burden and enhancing compliance for sites and study teams. This innovative solution empowers study teams to facilitate patient participation in clinical trials more effectively.

Through a user-friendly interface, learn how participants can access crucial information and complete consent electronically, improving efficiency and ensuring regulatory adherence, by downloading the datasheet below.

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