Get the right participants in your trial.
Content customized to your clinical trial using plain language and clear communication
All IRB-required elements, including study purpose, procedures, and potential risks and benefits
Patients engage with CONSENTER’s customizable on-screen avatar, who explains the trial process
Ensure consistent consent delivery across multiple sites and investigators, reducing staff burden
Deployment options ranging from tablet-based apps to eConsent integration
Multiple languages available, including American Sign Language (ASL)
Get the right participants in your trial.