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WE WANT YOU TO KNOW (ABOUT INFORMED CONSENT) In the vast majority of orthodontic cases significant improvements can be achieved. While the benefits of a pleasing smile, face and healthy dentition
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Informed consent is the process by which a patient or research subject is informed about and understands the risks and benefits of a medical treatment or research study before agreeing to participate.
Healthcare professionals, researchers, and institutions conducting medical treatments or research studies are required to obtain and file informed consent.
Informed consent forms typically include information about the purpose of the treatment or study, potential risks and benefits, alternatives, and the patient's right to ask questions or withdraw consent.
The purpose of informed consent is to ensure that patients or research subjects are fully informed about their participation in medical treatments or research studies, and to protect their rights and autonomy.
Information such as the nature of the treatment or study, potential risks and benefits, alternatives, confidentiality, and the right to withdraw consent must be reported on informed consent forms.
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