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Int. J. Harm. Sci. Rev. Res., 61(2), March April 2020; Article No. 05, Pages: 2327ISSN 0976 044XReview Article Importance of Informed Consent Form and Use of Electronic Informed Consent Form Dr. Mujeeb
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How to fill out importance of informed consent

01
Explain the purpose of the study or procedure to the participant.
02
Provide all necessary information about the risks and benefits involved.
03
Allow the participant to ask questions and clarify any doubts.
04
Ensure that the participant understands and agrees to participate voluntarily.
05
Have the participant sign the informed consent form to document their understanding and agreement.

Who needs importance of informed consent?

01
Anyone involved in medical research or clinical trials.
02
Patients undergoing medical procedures or treatments.
03
Individuals participating in psychological studies or experiments.
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The importance of informed consent is to ensure that individuals are fully aware of the risks and benefits of participating in a study or medical procedure before giving their consent.
Researchers, healthcare providers, and institutions conducting studies or medical procedures are required to obtain and file informed consent.
Informed consent forms typically include information about the study or procedure, risks and benefits, confidentiality, and the right to withdraw consent at any time. It is important to provide this information clearly and thoroughly.
The purpose of informed consent is to protect the rights and well-being of individuals participating in studies or medical procedures, and to ensure that they are making an informed decision.
Informed consent forms should include details about the study or procedure, risks and benefits, confidentiality, voluntariness, and contact information for questions or concerns.
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