Patient safety starts with the patient’s understanding of the trial and all of the inherent risks involved. This is where eConsent can offer more protection through a directed online experience. The step-by-step process guides the patient to ensure understanding and presents a signature box only at the end of these exercises.
Paper-free, fully electronic patient informed consent forms
Easy tracking of consent versions and which consent has been signed by what patient
Sign, countersign and revoke consent capability
Automatic creation of patients in EDC and/or ePRO after signing of eConsent
Multiple reports and exports available
Maximize Patient Retention
Paper-free informed consent will not only improve quality and compliance but retention for your clinical trial. eConsent provides patients with clear and understandable clinical trial information so you can make sure that they are fully informed when making a decision to participate in your trial. This saves not only time, which is critical for optimal launch timeframes, but money for your budget.
Create Cost Savings
Sponsors can achieve tremendous time and cost savings using eConsent by eliminating the costs involved in chasing, managing, and storing a paper trail. This further reduces the research team’s time involved in the consent process.
eConsent provides real-time tracking of recruitment rates to study sponsors. This is very important to get a consolidated view of study progress and also to not risk going over set enrollment goals.
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Next-generation patient data collection for validated questionaries on patients own phone, or Replior provided pre-installed phones.