Medidata eConsent is an advanced electronic consent system designed for clinical trials. It empowers patients to understand trial objectives and provide consent through multimedia technology, either onsite or remotely. This innovative solution automates patient enrollment, integrates with Rave EDC, and improves consent tracking management while reducing errors and administrative burdens for study teams.

Key Features

Multiple Ways to Engage Offers flexibility for patients to provide consent at the site or remotely, depending on study design.

• On-site consent option
• Remote consent capability

Integrated with Rave EDC Seamlessly unified with the Medidata Platform, used by the majority of clinical trials worldwide.

• Direct patient onboarding into Rave EDC
• Simplified integration compared to competitors

User-Friendly Configuration Tools Streamlines the setup process, reducing timelines and eliminating the need for extensive technical support.

• No developer support required
• Decreased study and site set-up timelines

Benefits

Enhanced Patient Experience Improves patient understanding, compliance, and engagement in clinical trials.

• Easy-to-understand clinical trial information
• Increased patient retention and compliance

Unified Platform Approach Offers seamless integration with the widely-used Medidata Platform.

• Simplifies workflow across clinical trial processes
• Reduces complexity in data management

Support for Decentralized Studies Enables flexible consent capture for hybrid and fully decentralized clinical trials.

• Location-independent consent capture
• 100% BYOD (Bring Your Own Device) support