1. Protection of Human Rights in Research
Haber, (2011), the informed consent is a voluntary consent that is required by a researcher to obtain participation from the participant in a clinical study, after informing them of all medical facts, risks and benefits involved in the research study. ... It defines the purpose of the study, the risks and benefits of the study, discomforts, how long the study will take place, location, how research will be conducted. ... This ensures that the research participants are informed of the potential risk of the study and are protected from those risks (Twomey, 2008). According to Provision three of ...
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- Grade Level: Undergraduate