Patient Engagement SmartSignals eConsent A patient-centric approach for a better overall experience What informed consent means Clinical trials achieve informed consent by providing comprehensive information to the potential study participants, so they understand their role and what to expect. Electronic consent can help you do this more efficiently than traditional, paper-based processes. In addition to increasing participant comprehension, electronic consent improves regulatory compliance and reduces data quality risks. You no longer have to stress about multiple protocol amendments – electronic consent takes care of the version control for you. eConsent Gather informed signatures from around the world faster than ever before.