Medidata Adds Video eConsent
Medidata, a Dassault Systèmes company, announced the addition of myMedidata eConsent, which enables video visits with patients and study staff. With video eConsent, trial participants can engage in remote, face-to-face, live conversation between patients and clinical trial site staff during the informed consent process. This expansion of the company’s telemedicine/video visit capability is the most recent addition to the myMedidata portal designed to be a single patient platform for all patient-centered technology.
The benefits of enabling video interaction during eConsent include:
- Enhanced patient experience by allowing patients to engage with their clinical research team prior to consenting
- Improved consent tracking management, which reduces informed consent errors and eases the administrative burden for sites and study teams
- Accessibility through the myMedidata patient portal so that patients can virtually access all of their trial needs in one location with one login.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.
AI in Clinical Trials: A Long, But Promising Road Ahead
May 29th 2024Stephen Pyke, chief clinical data and digital officer, Parexel, discusses how AI can be used in clinical trials to streamline operational processes, the importance of collaboration and data sharing in advancing the use of technology, and more.
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