The consent process is so much more than just obtaining a signature – its ensuring study participants meet the study requirements and fully understand their role in the research while easing administrative burdens for sites and study teams.
With decades of experience supporting clinical trials, Signant Health designed Signant SmartSignals eConsent modules to educate participants, streamline the process, and eliminate the inspection issues common with traditional, paper-based methods.
Screen potential study participants faster
Run a remote or hybrid study
Promote better participant engagement
PROOF AT THE SPEED OF LIFE
Signant SmartSignals eConsent
INCREASE COMPREHENSION & COMPLIANCE
eConsent solutions to support any study
Flexible licensing and implementation options give you the freedom to choose a solution that best fits your study's needs. Control the implementation process with Gold or Platinum's self-service implementation option, or work with our eConsent specialists who will handle the design and implementation process for you. All options support global remote consent for traditional, virtual, or hybrid studies but have important differences to consider.
Our solutions are better together
UNLOCK THE FULL VALUE OF eCONSENT
eCOA
PATIENT
CONCIERGE
SENSORS &
WEARABLES
TELEMEDICINE
Use one of our eConsent licenses as a stand-alone solution or combine with others in our comprehensive clinical trial evidence generation ecosystem for a fully streamlined, end-to-end digital experience
