Office for Human Research Protections (OHRP)
1. There are two types of clinical studies, i.e., clinical trials and observational studies. How do they differ and provide examples of each?
2. Who can participate in a clinical study and what is the process to protect them from harm?
Be sure in your initial response to provide at least two examples from peer reviewed literature that helps to support your position (write 5-6 sentence summaries for
Note: One outside source and the textbook source Textbooks: Fleming, S. T. (2008). Managerial epidemiology: Concepts and cases (2nd ed.).Chicago, IL: Health
Administration Press. ISBN 13: 978-1-56793-292-8