CLINICAL TRIAL PATIENT TECHNOLOGY INSIGHTS

ECOA RESOURCES

ECONSENT RESOURCES

  • Support the digitization of the participant consent process and begin creating multimedia-enhanced electronic informed consent forms (eICFs) that participants sign electronically, eliminating burdensome and error-prone paper-based processes.

  • Discover how DCTs leverage “virtual” tools, such as telemedicine, sensory-based technologies, wearable medical devices, and direct delivery of study drugs and materials to patients’ homes.

  • This on‑demand session offers a clear, practical overview of the major eSignature types used in eConsent — ranging from simple electronic signatures to fully qualified electronic signatures — and explains when each is appropriate.

EPRO RESOURCES