In certain situations, clinical research participants may not be able to provide informed consent themselves. In those cases, caregivers or legally authorized representatives can provide consent on their behalf, but a paper-based consent process introduces additional challenges.

This case study explains how a sponsor leveraged Signant’s eConsent solution to help a legally authorized representative provide remote consent and reconsent, enabling a comatose participant to be enrolled in a study and receive investigational treatment.

Download the case study to learn more about the challenges and results.