Patient eConsent

Clinical StudyPal’s eConsent feature automates the patient enrollment process and on-boards patients faster. The importance and benefits of eConsent include, but are not limited to: -Efficient use of time via automation, leading to a reduction of costs -Automation also speeds up the study’s start-up process -Reduces informed consent errors -Unique ability to consider multiple government regulations -Ability to configure for multiple language, increases the chances to reach a diverse population -Remote consent monitoring/remote patient monitoring -Creates a seamless and user-friendly experience, increasing patient compliance and patient retention -Guaranteed signature compliance -Allow patients to provide a hand signature or video consent -eConsent can lead to a transformative experience for study participants by providing simple, easy-to-comprehend clinical trial information, which will boost patient engagement and therefore improve the patient experience overall.