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INFORMED CONSENT FORM This is a clinical study, Frat University, Faculty of Dentistry which is conducted by Assist. Prof. Dr. Tapir Kara man, Assist. Prof. Dr. Eye Atlanta, Assist. Prof. Dr. Begin
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How to fill out informed consent form

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Step 1: Read the informed consent form carefully and understand its content.
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Step 2: Fill out your personal information, such as your name, age, and contact details.
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Step 3: If applicable, provide any relevant medical history or information that the form asks for.
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Step 4: Review the purpose of the study or procedure that the informed consent form is related to.
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Step 5: Go through the potential risks and benefits section and make sure you understand them.
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Step 6: If you have any questions or concerns, don't hesitate to seek clarification from the healthcare provider or researcher.
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Step 7: Sign and date the form to indicate that you have voluntarily agreed to participate or give consent.
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Step 8: Submit the filled-out informed consent form to the appropriate party as instructed.

Who needs informed consent form?

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Informed consent forms are required for anyone participating in a research study or clinical trial.
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Patients undergoing medical procedures or treatments may also need to sign informed consent forms.
03
Informed consent forms may be necessary for certain legal or professional situations, such as legal waivers.
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It is important to have informed consent from individuals who are involved in any activity that carries potential risks or consequences.
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Informed consent form is a document that provides detailed information about a research study or medical procedure and ensures that the individual understands the risks and benefits before agreeing to participate or undergo the procedure.
Researchers, healthcare providers, or any individual conducting a study or medical procedure involving human subjects are required to file an informed consent form.
To fill out an informed consent form, the individual must read all the information provided, ask any questions they may have, and then sign the form to indicate their understanding and agreement.
The purpose of informed consent form is to protect the rights and welfare of individuals participating in research studies or medical procedures by ensuring that they have all relevant information needed to make an informed decision.
The informed consent form must include details about the study or procedure, risks and benefits, confidentiality of information, voluntary participation, contact information for questions, and potential alternatives.
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