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U.S. NAVAL ACADEMY MIDSHIPMEN DEVELOPMENT CENTER INFORMED CONSENT AND LIMITS OF CONFIDENTIALITY STATEMENT PRIVACY ACT STATEMENT: Authority: U.S.C 301, Departmental Regulations, 10 U.S.C. 5013, Secretary
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Read through the informed consent form carefully to understand all the information and requirements.
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Sign and date the informed consent form to indicate your agreement and understanding.
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Make sure to ask any questions or seek clarification on any points that are unclear before signing the form.
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Ensure that all necessary information is filled out completely and accurately in the informed consent form.
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Be aware of any limits or restrictions specified in the informed consent form and adhere to them accordingly.

Who needs informed consent and limits?

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Informed consent and limits are typically required in situations where individuals are participating in research studies, medical procedures, or other activities that involve potential risks or consequences.
02
Patients, research participants, and individuals undergoing specific treatments or interventions are all examples of who may need to provide informed consent and be informed of any limits or restrictions.
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Informed consent is a process by which a participant gives permission for the use of their data or participation in a study after being fully informed of its purpose and potential risks. Limits refer to the boundaries defined around the use of that consent, such as what data can be shared and for how long.
Researchers, healthcare providers, and organizations conducting studies or treatments involving human participants are required to file informed consent and limits.
To fill out informed consent, individuals must provide clear and detailed information about the study, including its purpose, procedures, risks, and benefits, as well as the limits regarding data use. Participants must then sign the document to indicate their agreement.
The purpose of informed consent and limits is to ensure that participants are fully aware of the study they are participating in, understand their rights and the extent of their participation, and give voluntary permission without any coercion.
Information that must be reported includes the study's purpose, procedures, risks and benefits, confidentiality assurances, and the participant's right to withdraw at any time without penalty.
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