Join the next generation of clinical researchers streamlining their trials with Smart Omix eConsent.
Engagement. Empowerment. Efficiency. eConsent has never been this easy.
With Smart Omix eConsent, you can both engage your participants with a highly personalized user experience and streamline clinical trial recruitment with an efficient consent process. This is consent for the 21st century.
Simplify patient participation with customizable language and configurable multimedia components.
Shape your patient’s experience with personalized language, images, audio, and videos. Our robust eConsent modules make it incredibly easy to boost retention before even beginning the study.
Empower your participants with knowledge checks.
Our consent comprehension screen ensures your participants fully understand why they are participating and optimize the integrity and quality of your Informed eConsent.
Incorporate your consent language with a simple copy- and-paste.
It really is that easy. Eliminate errors with our intuitive, easy-to-use consent screen which allows you to simply copy-and-paste your study’s IRB-approved consent language
Enjoy 21 CFR Part 11 compliance.
Our eConsent module is 21 CFR Part 11 compliant, with industry-best standards in place for digital signature collection.
Automated delivery of signed eConsent forms.
Researchers and participants are immediately emailed a copy of signed eConsent forms.
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