In Undergraduate Biomedical Engineering Curriculum at NJIT, students are required to take the Capstone (Senior Design Project) Class. If the project involves testing on human subject, an IRB approval is required prior to conducting the experiment.

I feel like we conduct experiments in school, but not necessarily clinical trials. Share an experience whether in school or industry, when you have executed the clinical trial protocol? How is it different from the clinical trial protocol that we learned in this week’s lecture?