Fully Integrated, Participant-Friendly eConsent for Today’s Clinical Trials

Speakers

• Richard Murg, Global Vice President, Business Development, Bioclinica Software Solutions
• Blain Young, Pre-Sales Solutions Consultant, Bioclinica Software Solutions

Digital processes such as eConsent are becoming essential for today’s clinical trials. However, there’s more to consider than just asking participants to electronically sign a consent form. Integrating eConsent into trials spans form design, sponsor and institutional review board (IRB) approvals, as well as site and participant ease of use.
In this webinar, representatives from Bioclinica discuss these considerations and demonstrate how Bioclinica eConsent enables an electronic informed consent process from start to finish, including:

• Improved participant understanding by integrating other digital technologies such as videos and voiceovers into the informed consent process
• Reduction of site burden with an intuitive interface
• Incorporating IRB review and approval into the system itself