10 FAQs On eConsent

In the life science sector's digital transformation, eConsent replaces traditional paper-based processes, simplifying consent for patients, sponsors, and site staff. This shift streamlines administrative tasks, enhances trial efficiency, and fosters a collaborative environment through user-friendly interfaces and multimedia features.

Overall, eConsent signifies a crucial move towards a patient-centric, efficient, and technologically advanced approach in clinical trials, aligning with the broader trend of digitalization in the life sciences and addressing the challenges of traditional consent methods. However, there are many intricacies surrounding the electronic consent forms.

In this article, we provide ten inquiries to further examine the challenges of adoption, integration, and compliance measures, offering valuable insights for those contemplating the incorporation of eConsent in clinical trials.