Get the FREE AND INFORMED CONSENT
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AC.4.4.2
FREE AND INFORMED CONSENT
Section:
Subject:Academic/Student (AC)
Applied ResearchLegislation:
Effective:
Revision:January 21, 2005,
January 20, 2006; January 29, 2013; September 1, 2016 (reformatted)APPROVED:President
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What is and informed consent?
Informed consent is a process where a patient or participant in a research study is provided with detailed information about the study, including the risks and benefits, before agreeing to participate.
Who is required to file and informed consent?
Researchers, healthcare professionals, and individuals conducting studies or clinical trials are required to obtain and file informed consent from participants or patients.
How to fill out and informed consent?
To fill out informed consent, the individual conducting the study or trial must provide detailed information about the study, including the purpose, risks, benefits, and any alternatives to participation. The participant must then sign the consent form to indicate their understanding and agreement.
What is the purpose of and informed consent?
The purpose of informed consent is to protect the rights and safety of research participants or patients by ensuring they have all the necessary information to make an informed decision about participating in a study or trial.
What information must be reported on and informed consent?
Informed consent must include information about the purpose of the study, potential risks and benefits, confidentiality of data, contact information for questions, and the participant's right to withdraw from the study at any time.
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