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Review the informed consent document thoroughly.
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Who needs informed consent - genomegov?

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Anyone participating in a research study that involves the collection and analysis of genetic information should have informed consent.
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Informed consent is a process in which a person is given all relevant information about a research study and agrees to participate voluntarily.
Researchers conducting studies that involve human subjects are required to file informed consent.
To fill out informed consent, researchers must provide detailed information about the study, risks, benefits, and ensure participants understand before they can sign the consent form.
The purpose of informed consent is to respect an individual's autonomy, promote transparency in research, and ensure participants have enough information to make an informed decision about participation.
Informed consent forms must include details about the study purpose, procedures, risks and benefits, confidentiality, voluntary participation, and contact information for questions.
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