Speakers
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: