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1990 2020EARSAPIL webinars CELEBRATING 30Informed consent: Part one Monday, 9 November 2020 12:00 13:00 These seminars explore the burgeoning area of informed consent in clinical negligence litigation
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Informed consent is the permission given by a patient to a healthcare provider for a specific medical intervention or treatment.
The healthcare provider is responsible for obtaining and documenting informed consent from the patient.
When filling out informed consent, the healthcare provider must ensure all risks, benefits, and alternatives to the treatment are clearly explained to the patient.
The purpose of informed consent is to ensure that the patient understands the treatment being recommended, including potential risks and benefits, before making a decision.
Informed consent forms typically include information about the specific treatment, potential risks, benefits, and alternatives, as well as the patient's acknowledgment of understanding.
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