Clinical Trials are often driven by specific endpoints and clinical events. In the context of such trials, there a need to perform such endpoint determinations in a standardized fashion using validated definitions.
Webinar
This session will provide a summary of eConsent features that can support metrics capture along with a more general discussion of how to design a study (or studies) to test the efficacy of eConsent.
Dr. Fuad Abujarad will present the new digital health tool, VIC, to complete the informed consent process.
In 2018 The Multi-Regional Clinical Trials Center of Brigham and Women’s Hospital and Harvard assembled a workgroup of key clinical research stakeholders to tackle the issue of how to better integrate health literacy into the clinical research process.
IRB Reliance Exchange (IREx) is the single IRB portal used by the TIN Single IRBs (SIRBs). It can also be used to support any IRB serving as the SIRB and non-TIN studies.
Vanderbilt has recently developed a generalizable solution for supporting studies requiring patient-centered mobile applications.