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Jefferson Office of Human Research Informed Consent OHR8 Version Date FOR OH RUSE: 11/1/18Department:Principal Investigator:Study Title:To complete this consent form, please modify it as appropriate
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How to fill out informed consent faqshhsgovinformed consent

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To fill out informed consent form, follow these steps:
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Read the form carefully and understand the information provided.
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Ask any questions to clarify any doubts or concerns.
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Provide your personal information accurately and completely.
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Check the boxes or provide your consent to specific sections as required.
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Date and sign the form to indicate your agreement and understanding.
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Keep a copy of the consent form for your records.

Who needs informed consent faqshhsgovinformed consent?

01
Informed consent is typically required for any individual who will be participating in a research study or medical procedure.
02
This includes patients, volunteers, or subjects who will be involved in the study or procedure.
03
Informed consent ensures that individuals have been fully informed about the risks, benefits, and potential consequences of their participation.
04
It is an important ethical principle to protect the rights and autonomy of individuals involved in any form of research or medical intervention.

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Informed consent is a process for getting permission before conducting a healthcare intervention on a person.
Healthcare providers and researchers are required to obtain informed consent from patients or participants.
To fill out informed consent, the healthcare provider or researcher must provide information about the treatment or study, risks and benefits, and answer any questions the patient or participant may have.
The purpose of informed consent is to ensure that the patient or participant understands the treatment or study, risks involved, and agrees to participate voluntarily.
Informed consent must include information about the treatment or study, risks and benefits, confidentiality, alternative treatments, and the right to withdraw consent.
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