SmartSignals eConsent Facilitates Consent in Emergency Situations Date Published: Feb 28, 2022 Case Study 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. Download Share: LinkedIn0Tweet0 Recommended Resources SmartSignals eConsent Download Now Brochure Decentralized Clinical Trial Solutions Download Now Brochure Scaling Up eConsent in Traditional & DCTs Watch Now Webinar