The discussion for this week is focused on preparation for your IRB application. What are the important considerations in the protection of human subjects and confidential information in your project? How will you assure an ethical and protective process for all involved in this project, including patients and other stakeholders?
Please give an update on your project status. Is IRB approval required from your project site? If so, have you started this process? If not, do you have a letter from the site stating that IRB is not required?
When posting, please first share your PICOT question in question format and then respond to the weekly question. This will help us all to be able to provide quality feedback in these weekly discussions.
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