Transforming Patient Consent in a Global Oncology Trial
This case study demonstrates how a global biopharma company implemented our eConsent solution to overcome complex consent challenges in a multinational breast cancer study spanning 6 countries and 8 languages.
The solution transformed cumbersome 60+ page paper forms into an interactive multimedia experience, allowing remote review and capturing specific discussion points for investigator conversations.
For study teams, the platform streamlined IRB submissions with comprehensive documentation packages while providing real-time insights into patient engagement metrics across all 55+ sites.
Download to discover how eConsent technology can reduce administrative burden while improving patient understanding and compliance documentation in your global clinical trials.
