Understand the current regulations and guidance related to vulnerable subjects while learning methods for practical application in your daily activities. New threats to the vulnerable arise and corresponding regulation and guidance evolve to address them. The speaker will provide insights on the importance of maintaining a contemporary understanding of vulnerable subjects and adjusting perceptions in order to protect vulnerable subjects in clinical trials.
Recount the basic ethical and regulatory components that apply to protection of the vulnerable in research
Interpret the changing regulatory landscape as it applies to the pretection of vulnerable populations and individuals
Incorporate these into a contemporary framework that can be applied to protect the vulnerable specific to each research professional's individual role in the research enterprise