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CONNIE CASED, MD INFORMED CONSENT REGARDING EMAIL, TEXTING AND/ OR INTERNET USE OF PROTECTED PERSONAL INFORMATION Connie Casey, MD provides patients the opportunity to communicate with their practitioner
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Informed consent is needed by anyone participating in a research study, clinical trial, or medical procedure where potential risks are involved.
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Informed consent is regarding a process whereby a patient is fully informed about the benefits and risks of a medical procedure before deciding whether to undergo it.
Healthcare providers are required to obtain informed consent from patients before performing any medical procedure.
To fill out informed consent, healthcare providers must provide detailed information about the procedure, risks, benefits, and alternatives to the patient.
The purpose of informed consent is to ensure that patients are fully aware of the implications of a medical procedure and can make an informed decision about their healthcare.
Informed consent must include details about the procedure, associated risks, potential benefits, alternative treatments, and the patient's right to refuse treatment.
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