Discussion Post
a) Describe what an IRB is and how research is approved.
b) Comment on regulatory protections of human subjects in research, and most particularly when IRB approval is needed.
c) Include two examples of human research studies that went awry, and the lessons learned from those examples.
The response must include a reference list. Using one-inch margins, double-space, Times New Roman 12 pnt font and APA style of writing and citations.