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NAU IRB Approved: 8/16/2013 Revised IC approved: 10/15/2014 Valid until: 8/14/2015-Page 1 of 4Human Subject Informed Consent Department of Communication Sciences and Disorders 208 E. Pine Knoll Drive,
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Informed consent instructions ampamp are guidelines provided to individuals to ensure they understand the risks and benefits involved in a particular situation before they give their consent.
Healthcare professionals, researchers, and individuals conducting studies or procedures that involve obtaining informed consent are required to file informed consent instructions ampamp.
To fill out informed consent instructions ampamp, one must provide detailed information about the procedure or study, clearly outline the risks and benefits, and ensure the individual understands and agrees to participate.
The purpose of informed consent instructions ampamp is to protect the rights and well-being of individuals by ensuring they have all the necessary information to make an informed decision before participating in a study or procedure.
Informed consent instructions ampamp must include details about the study or procedure, risks involved, benefits expected, alternative options, confidentiality measures, and the right to withdraw consent at any time.
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