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Informed Consent Patients surname: First name: Date of birth: Acknowledgement of informed consent and agreement to specialized orthodontic treatment: 1. Informed consent The orthodontist treating
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Read the informed consent form thoroughly to understand its purpose, risks, benefits, and any alternatives.
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Provide your personal information accurately, including your name, date of birth, and contact details.
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Understand the purpose of the research or medical procedure for which you are giving consent and ask any questions you may have.
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Who Needs Informed Consent - BMedB-BCollegeBDe:

01
Patients or participants involved in medical research studies, clinical trials, or experimentation.
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Individuals undergoing medical procedures, including surgeries, treatments, or therapies that carry potential risks.
03
Participants in mental health or counseling sessions where sensitive information may be disclosed.
04
Individuals participating in studies involving the collection of personal information or biometric data.
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Minors or individuals who may lack decision-making capacity often require a legal guardian's or parent's consent.
Note: It is essential to consult with a legal professional or healthcare provider for specific guidance regarding informed consent in your jurisdiction.
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Informed consent is a process for getting permission before conducting a healthcare intervention on a person.
Healthcare providers are required to obtain informed consent from patients before performing any medical interventions.
Informed consent forms are typically filled out by the healthcare provider and signed by the patient or their legal guardian.
The purpose of informed consent is to ensure that patients have all the necessary information to make an informed decision about their healthcare treatment.
Informed consent forms must include information about the nature of the treatment, potential risks and benefits, and alternative options.
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