Once an informed consent is obtained, the researcher is no longer liable if actual harm results from the research.
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Q31: Some researchers believe that concealment or deception
Q32: Debriefing should be done without demeaning the
Q33: Debriefing should always be done with research
Q34: When using a placebo control group, the
Q35: If an experimental treatment significantly, positively affects
Q37: Experimental research has greater ethical risks than
Q38: Focus groups pose special confidentiality problems because
Q39: All institutional research that systematically collects data
Q40: The Institutional Review Board is not obligated
Q41: If the researcher changes the procedure or
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