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MISSISSIPPI STATE UNIVERSITY Management of RPP Documents (0101) HUMAN RESEARCH Approved 08.12.2015 PROTECTION PROGRAM Purpose The purpose of this Standard Operating Procedure (SOP) is to define how
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Who needs management of hrpp documents:
01
Researchers conducting human subjects research: Researchers who are involved in studies or projects that involve human subjects need to have proper management of hrpp documents. This ensures that the welfare and rights of the participants are protected, and ethical standards are followed.
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Institutional Review Boards (IRBs): IRBs play a crucial role in the management of hrpp documents as they review and approve research protocols involving human subjects. They rely on accurate and complete documentation to make informed decisions about the ethical acceptability of research.
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Regulatory authorities: Regulatory authorities, such as government agencies or ethics committees, may require management of hrpp documents as part of their oversight responsibilities. They ensure compliance with applicable regulations and help safeguard the rights and well-being of human subjects.
In summary, filling out management of hrpp documents requires careful attention to detail and compliance with applicable regulations. Researchers, IRBs, and regulatory authorities are among the stakeholders who need these documents to ensure ethical conduct and protection of human subjects in research.
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What is management of hrpp documents?
Management of hrpp documents refers to the process of organizing, storing, updating, and maintaining all documents related to Human Research Protection Program.
Who is required to file management of hrpp documents?
All researchers and institutions involved in human subjects research are required to file management of hrpp documents.
How to fill out management of hrpp documents?
Management of hrpp documents can be filled out electronically or manually, following the guidelines provided by the regulatory authorities.
What is the purpose of management of hrpp documents?
The purpose of management of hrpp documents is to ensure transparency, accountability, and compliance in human subjects research.
What information must be reported on management of hrpp documents?
Management of hrpp documents must include details such as study protocols, informed consent forms, IRB approvals, and any amendments or adverse events.
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