While the shift to digitizing the clinical trial process is underway, the informed consent process for clinical trials generally has been paper-based. With the exponential number and increasing complexity of clinical studies now being run the paper-based informed consent process is inherently inefficient. The benefits of eConsent include an ability to provide patients clear and easy-to-understand clinical trial information, improved patient compliance, a reduction in inspection findings and enable process efficiencies.
Rave eConsent is an innovative, patient-friendly, electronic informed consent and patient enrollment system for clinical trials. Through the use of multimedia technology, patients are educated and guided through key elements of a clinical trial. eConsent can be used for clinical study consents, assents, disease registries, biobanking registries. eConsent allows the patient, sites, CRO and sponsor a unified experience for enrollment while providing additional study analytics to the site and CROs.