Published by
@ShahidNShah
@ShahidNShah
As the first stage in enrollment in a clinical trial, the consent form plays a key role in patient engagement
Clinical / Medical Research Patient Engagement Science and Research (Medical Devices)
Kayentis has chosen to add an electronic Informed Consent Form (eICF) to its eCOA solution to improve patient engagement from the moment of inclusion in a clinical trial. Simplifying e-consent, SecureConsent® developed by our strategic alliance partner offers an easy-to-understand consent form, with audio of the approved consent in the patients language, embedded information for specified concepts, and electronically captured handwritten signature capability.
SecureConsent® developed by our strategic alliance partner offers several benefits for a patients understanding and compliance, while maintaining adherence to regulations:
Improves patient comprehension and ultimately compliance and commitment.
Improve consistency and quality about a delivery, tracking, monitoring, and archiving all relevant, informed consent information in a searchable database.
Provides trial staff with a real-time high-level overview of the trial consent process at all sites.
Improves the quality and efficiency of interactions between patients and site staff.
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