Webinar: Questions in Everyday IRB Deliberations: An Interactive, Case-Based Approach

When:  Sep 21, 2023 from 13:00 to 15:00 (ET)

IRB review of human subjects research consistently presents a wide variety of ethical and regulatory challenges in even the simplest of research protocols. In this session, we will explore several of a wide variety of biomedical and social and behavioral science studies, and parse out the often thorny ethical and regulatory issues that are part and parcel of an IRB’s everyday reviews.

Potential topics include ethical justification for randomized clinical trials; use of placebo; fCOI; inclusion (and exclusion) of vulnerable subjects; phase 1 trials and risk-benefit analysis; compensation (and coercion) of subjects; optimizing informed consent; secondary research findings; data and safety monitoring; and assessment and minimization of risk.

This case study-based Zoom meeting offers attendees the opportunity to interact with the speakers and other participants on screen. Through a combination of active audience participation and very brief didactic episodes, the speakers will highlight the challenges, how those challenges fit within the regulatory criteria for approval, and best practices for review. Attendees will leave with a framework for IRB members and administrators to use in effectively reviewing protocols involving these thorny components.