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Patient Engagement

SmartSignals eConsent

A patient-centric approach for 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 texpectElectronic consent can help you do this more efficiently than traditional, paper-based processes.  

In addition to increasing participant comprehensionelectronic 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.