
Research involving children requires a careful balance between protecting a vulnerable population and enabling valuable scientific inquiry. This webinar provides you with actionable strategies for translating the regulatory requirements of 45 CFR 46, Subpart D into actionable, ethical procedures tailored for field research, especially with younger participants. The webinar also identifies areas where the regulations allow flexibility, highlights strategies for clear communication of Institutional Review Board (IRB) expectations, and examines effective collaboration between IRBs and researchers to ensure ethical and feasible study designs.
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