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I consent to participate in the research project and the following has been explained to me: the research may not be of direct benefit to me. my participation is completely voluntary. my right to withdraw from the study at any time without any implications to me.
What is a Consent Form? Consent forms, sometimes called release forms, are legal documents that serve as written permission to send or receive information among participating parties. They often inform them of associated use risks and release the provider from associated claims.
A consent form is a legal document that ensures an ongoing communication process between you and your health care provider.
Purpose of IRBs Institutional Review Boards, or IRBs, review research studies to ensure that they comply with applicable regulations, meet commonly accepted ethical standards, follow institutional policies, and adequately protect research participants.
The consent form provides potential research subjects sufficient written information to decide whether to participate in a research study or not based on an explanation of the proposed research and the nature of the participation that is requested of them.
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Informed consent is fundamental to the conducting of ethical research. An informed participant understands the implications of taking part in the research and they agree to be a part of the research; participation voluntary and they can withdraw at anytime.
The fundamental purpose of IRB review of informed consent is to assure that the rights and welfare of subjects are protected.
Informed consent means that the purpose of the research is explained to them, including what their role would be and how the trial will work. A central part of the informed consent process is the informed consent document.

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