Research is needed to improve conditions. Prepared for any research is likely to help the company directly or indirectly. Before starting data collection, researchers must inform and obtain consent from participants. Say no to plagiarism. Get a tailor-made essay on "Why Violent Video Games Shouldn't Be Banned"? Get an Original Essay The meaning of informed consent is an essential part for researchers reaching out to participants before carrying out research. Informed consent means that participants are aware of the type of information that is wanted from them, why the information is being requested, what it will be done for, how they are expected to participate in the study, and how this directly affects about them. It is important to obtain consent on a voluntary basis and without any pressure on the participants. The information elements of the participants' consents must be noted in full. The topic must be confidential and anonymous. The informed consent form must be written in lay language to make the research participants easily understandable. The researcher must allow time to answer questions available to participants at all times. The elements of consent must be voluntary without any pressure. Participants must also be free to withdraw consent at any time they wish. The consent form must contain an explanation of the purpose of the research project, how the study will be conducted, harm and risk, value and benefit, in private. , refusal from the study, hard statement, consent form and the last thing must be signed by the participants. A human subject is defined as a living person about whom the investigator conducting the research will receive information. This includes the study of human beings through surveys or interviews, psychological, physiological or medical tests or treatments, observation, access to their personal records or other materials such as the collection and use of their organs, tissues or body fluids . Access to their details is a form of personally identifiable confidential information as part of a published source or existing database. A related issue with this is the risk of the research to participants. A risk can cause harm, discomfort or inconvenience. The list of damages is not exhaustive but may include physical damages such as injury, illness and pain. Psychological damage represented by feelings of worthlessness, anguish, guilt, anger or fear. For example, disclosure of sensitive or embarrassing information, or knowledge of the genetic possibility of developing an incurable disease. Devaluation of personal worth such as being humiliated, manipulated, or treated disrespectfully or unfairly. Social harm, including harm to social networks or relationships with others, discrimination in access to benefits, services, employment or insurance, social stigmatization, and establishment of unknown prior paternity status. Economic harm including the imposition of direct or indirect costs on participants. Legal harm: including the discovery and prosecution of criminal conduct. The discomfort is less serious than the damage and can involve the physical and mental body. Examples of minor side effects of medications, discomfort related to venipuncture, anxiety induced by an interview. When a person's reactions exceed discomfort and become distress, they should be considered harm. Less serious than discomfort is an inconvenience. Examples of inconveniences may include having to travel to participate in the research, fill out a form, participate in a survey, or give up time to participate in the research. Research can also involve,.