eConsent

The eConsent system by EvidentIQ enhances the experience of trial participants by providing an entirely electronic informed consent process. It aims to improve the quality and efficiency of clinical trials by offering insights into the patient experience and ensuring high data quality.

Traditional paper-based informed consent can lead to misunderstandings and inconsistent communication. eConsent addresses these issues by presenting information electronically, potentially including multimedia elements like images, audio, video, and diagrams. This format aids comprehension and facilitates the consenting process with less effort.

Features

• Ease Workload for Study Teams and Sites: Simplifies and accelerates the consent process through a customized recruitment portal and pre-screening questionnaires. Automatically updates patient data in the EDC system post-consent.
• Enhancing Patient Understanding: Provides comprehensive information using embedded videos, graphics, and other multimedia, ensuring patients receive the most recent information.
• Regulatory Compliant Video Calling: Offers secure video consultations, minimizing the need for in-person visits and integrating seamlessly with the consent process.

Benefits

• eConsultation: Allows patients to contact study personnel directly for questions, enhancing transparency and understanding.
• eSignature: Compliant with 21 CFR Part 11 and Annex 11, ensuring secure and tamper-proof electronic consent.
• Full Control: Enables study personnel to interactively share media and address patient queries during consultations.
• eEnrollment: Automates EDC enrollment through EvidentIQ's extensive patient community.
• Provide a Multimedia Experience: Offers a wide range of design capabilities to guide participants through the consent process.
• Allow Participant Device of Choice: Accessible on any modern browser, enhancing participant engagement.