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INFORMED CONSENT AGREEMENT TEMPLATENOTE: One of the most common reasons for delay of IRB approval is an inadequate informed consent agreement. It is recommended that you follow this template, write
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An informed consent agreement template is a document that outlines the terms and conditions of a research study or medical procedure that a participant must agree to before participating.
Researchers, medical professionals, or institutions conducting the study or procedure are required to provide participants with an informed consent agreement template.
The informed consent agreement template should be filled out by the participant, indicating their understanding of the study or procedure, risks involved, and their voluntary agreement to participate.
The purpose of the informed consent agreement template is to ensure that participants are fully informed about the study or procedure they are taking part in, their rights, and any risks involved.
The informed consent agreement template must include details such as the purpose of the study, potential risks and benefits, participant rights, confidentiality, and contact information.
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