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IRB NUMBER: 13171EX IRB APPROVAL DATE: 11/22/2016 IRB EXPIRATION DATE: 11/21/2017INFORMED CONSENT AND HIPAA AUTHORIZATION TO PERMIT THE USE AND DISCLOSURE OF PROTECTED HEALTH INFORMATION (PHI) FOR

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How to fill out of 6 informed consent

01

Ensure that the participant is fully informed about the study objectives, risks, benefits, and procedures.

02

Use simple language that the participant can easily understand.

03

Provide ample time for the participant to review the consent form and ask any questions.

04

Clearly outline the voluntary nature of participation and the participant's right to withdraw at any time.

05

Obtain the participant's signature and date on the consent form.

06

Provide a copy of the signed consent form to the participant for their records.

Who needs of 6 informed consent?

01

Anyone participating in a research study or clinical trial that involves human subjects needs to fill out an informed consent form.

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What is of 6 informed consent?

Informed consent is a process for getting permission before conducting a healthcare intervention on a person.

Who is required to file of 6 informed consent?

Healthcare providers and researchers are required to obtain and file informed consent from patients before conducting any procedures or studies.

How to fill out of 6 informed consent?

To fill out informed consent, the healthcare provider or researcher must explain the nature of the procedure or study, the potential risks and benefits, and ensure the patient fully understands before obtaining their signature.

What is the purpose of of 6 informed consent?

The purpose of informed consent is to respect the autonomy of individuals and ensure they have the information needed to make informed decisions about their healthcare.

What information must be reported on of 6 informed consent?

The informed consent form must include information on the procedure or study being conducted, the risks and benefits involved, alternative options, and the participant's rights.

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