What are your thoughts regarding these guidelines.
Are they necessary?
Why or why not?
Explain the different levels.
Are you familiar with IRBs?
Do you have an IRB at your institution?
How do they function?
How often do they meet?
What are the general requirements for an informed consent?
The International Council of Nurses’ (ICN) The ICN Code of Ethics for Nurses (2012)
American Nurses Association’s (ANA) ANA Position Statements on Ethics and Human Rights
ANA’s Code of Ethics for Nurses
Steneck, N. (2007). ORI introduction to the responsible conduct of research. Washington, D.C.: US Government Printing Office.
The Hastings Center web site
The Hastings Center’s Bioethics Forum
Office for Human Research Protections (OHRP)
Office for Human Research Protections (OHRP) IRB guidebook
U.S. Department of Veterans Affairs, Human Subjects Protection
Collaborative Institutional Training Initiative (CITI)
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