Simplify And Elevate The Participant Consent Process With iMednet

The Electronic Informed Consent (eConsent) feature of iMednet was created as an integral part of the iMednet platform, enabling seamless integration to ensure a secure, straightforward, and efficient electronic consent process for both study participants and site users.

It was thoughtfully designed to accommodate the diverse requirements of traditional, hybrid, and decentralized clinical trials so that participants have the flexibility to review and provide consent at their convenience, anytime and from anywhere, whether they're using a smartphone, tablet, or computer.

Explore the ways that this responsive design guarantees a user-friendly experience across all devices.