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INFORMED CONSENT STATEMENT The Impact of ABC on OXY in Young Adults Student Researcher: Jane Doe Jane.Doe@my.ccsu.edu Faculty Advisor: Dr. John Smith JSmith@ccsu.edu1. Invitation to Participate and
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Who needs informed consent statement?

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Anyone participating in a research study or clinical trial.
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Patients undergoing medical treatment or procedures.
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Informed consent statement is a document that explains the risks, benefits, and alternatives of a specific course of action to an individual and confirms their understanding and agreement.
Healthcare providers, researchers, and organizations involved in medical treatments and experiments are required to file informed consent statements.
Informed consent statements are typically filled out by providing detailed information about the procedure or treatment, risks involved, alternatives, and obtaining the signature of the individual acknowledging their understanding and agreement.
The purpose of informed consent statement is to ensure that individuals are fully informed about the risks and benefits of a medical procedure or treatment before they make a decision to proceed.
Informed consent statements must include information about the procedure or treatment, risks involved, benefits, alternatives, and the individual's agreement to proceed.
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