In social psychology: How might different regions in the US interpret ethical "harm" in a research lab?
Different regions in the US interpret ethical "harm" in a research lab in a way that is having consensuses regarding the following points;
The principle of voluntary participation requires that people should not be coerced into participating in research. The voluntary participation leads to the mandatory requirement of informed consent. The ethical standards also require that researchers should not put participants in a situation where they might be harmed as a result of their participation in a research. Almost all research guarantees the participants confidentiality.
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