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Premier Oral Surgery Sim 3 Simon 411 Barnu!Simon Bangiyev, DDS, MDDiplomate)of)the)American)Board)of)Oral)and)Maxillofacial)Surgery)!!!!!!!!!!!TOOTH!EXTRACTION!INFORMED!CONSENT! CONSENTIMIENTO INFORMADO
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Read the informed consent form carefully to understand the purpose, risks, benefits, and procedures involved in the study.
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If the participant is a minor or unable to provide consent, a legal guardian or authorized representative must sign the form on their behalf.

Who needs informed consent and permission?

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Anyone who is participating in a research study or clinical trial needs to provide informed consent and permission.
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Informed consent and permission is a process through which individuals are provided with clear, comprehensive information about a procedure or study, allowing them to make a voluntary and educated decision about their participation.
Researchers, healthcare providers, and institutions conducting studies involving human subjects are required to file informed consent and permission.
To fill out informed consent and permission, ensure that all pertinent information regarding the study, including purpose, procedures, risks, benefits, and the participant's rights, is clearly stated and understandable.
The purpose of informed consent and permission is to protect the rights and welfare of participants, ensuring they understand the implications of their involvement and can make informed choices.
The information that must be reported includes study objectives, procedures, potential risks and benefits, confidentiality assurances, and the participant's right to withdraw at any time.
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