Sage Bionetworks has developed a novel multi-media approach to addressing transparency and comprehension within electronic informed consent (eConsent) for app-mediated research studies. We deployed this eConsent process in minimal-risk research studies. Here we describe the rationale for the framework selected and best practice for application of the framework in other clinical studies.
OHRP eConsent Webinar
Use of E-Consent in Human Subjects Research: This is a recording of a webcast presentation to the Office for Human Research Protections (OHRP) on January...
Using Patient Data in Research: Balancing Benefits and Risks
What risks exist when companies carry so much consumer data? How can good practice and regulations mitigate these risks? Panelists discuss this during the Future...