Please, Reply to following with most recent

Please, Reply to following with most recent sources. In a research study, the intent is to contribute to universal knowledge, therefore it must be approved by the Institution Review Board (IRB). This Review Board is a committee of individuals who ensures that no harm is done to the individuals who are partaking in the study. Therefore, the research study requires IRB approval, informed consent from the participants, understanding of the risk to the participants, randomization process, validity and reliability (Helbig, 2018). An example of a research study is the harm and/or effects one medication may do to a participant as opposed to another medication. This may cause unknown side effects that may harm the patient in the short or long term, therefore there are regulations to this study. SCIENCE HEALTH SCIENCE NURSING HLT-362V O500

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