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1 IRB: Protocol #: Date: Reviewer: Informed Consent/Assent Checklist MAINE CDC holds a Federalize Assurance with the Office for Human Research Protections (formerly ORR), HHS, whereby MAINE CDC agrees

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What is informed consentassent checklist?

The informed consent checklist is a document that outlines the necessary steps and information required to obtain informed consent from individuals participating in a study or research project.

Who is required to file informed consentassent checklist?

Researchers, scholars, and professionals conducting studies or research projects that involve human subjects are typically required to file the informed consent checklist.

How to fill out informed consentassent checklist?

To fill out the informed consent checklist, the researcher must ensure that all the required information about the study, potential risks, benefits, confidentiality, and participant rights are clearly stated. The checklist should be signed and dated by both the researcher and the participant.

What is the purpose of informed consentassent checklist?

The purpose of the informed consent checklist is to ensure that participants have a clear understanding of the study's purpose, procedures, potential risks and benefits, as well as their rights as research subjects. It serves as a documentation of the informed consent process.

What information must be reported on informed consentassent checklist?

The informed consent checklist should include information such as the study's title, purpose, procedures, potential risks and benefits, confidentiality measures, contact information of the researcher, and space for the participant to ask questions and provide consent.

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