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IRB Approved: 3/4/2019 Approval Expires: 9/23/2019IRB#: 17123Research Consent Summary You are being asked to join a research study. You do not have to join the study. Even if you decide to join now,

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Who needs revised common rule qampampashhsgov?

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Researchers who are conducting studies involving human subjects

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Institutional Review Boards (IRBs) responsible for reviewing and approving research protocols

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Anyone involved in the research process that needs to comply with the revised common rule regulations

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What is revised common rule qampampashhsgov?

The Revised Common Rule, implemented by the U.S. Department of Health and Human Services, governs the protection of human subjects in research and outlines the requirements for institutional review boards (IRBs), informed consent, and registration of research studies.

Who is required to file revised common rule qampampashhsgov?

Researchers and institutions that conduct federally funded research involving human subjects are required to comply with the Revised Common Rule.

How to fill out revised common rule qampampashhsgov?

Filling out the Revised Common Rule involves completing forms that detail the research study, including the study's purpose, methodology, and informed consent procedures, as well as submitting them for approval to the relevant IRB.

What is the purpose of revised common rule qampampashhsgov?

The purpose of the Revised Common Rule is to enhance the protection of human research participants, promote ethical research practices, and ensure that informed consent is obtained appropriately.

What information must be reported on revised common rule qampampashhsgov?

Researchers must report information including study title, principal investigator, study description, risks, benefits, and procedures for ensuring informed consent, as well as data safety monitoring plans.

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