Consent Notifications Feature Focus

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Receiving consent from a patient is one of the most crucial parts of the clinical trial process. Without the consent of patients, research sites cannot move forward with their trials. This means that keeping track of consent forms for patients participating in a clinical trial is extremely important for sites.By promoting patient safety, as well as efficient record keeping for the trial, consent notifications allow sites to properly keep track of patient consent form status and be able to stay in compliance with the rules of the clinical trial.

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