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CPS HI Form Revised 06.26.2015University of Puerto Rico Mayaguez Campus Dean of Academic Affairs Institutional Review Boardman Subject Research Approval Form New Project Title of project. Main researcher

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How to fill out human subject research approval

01

Obtain the necessary forms and documents from the institution or committee overseeing human subject research.

02

Provide detailed information about the research project, including the purpose, methods, risks, and benefits to the subjects.

03

Obtain informed consent from all participants before starting the research.

04

Ensure that the research protocol follows ethical guidelines and regulations.

05

Submit the completed forms and documents to the appropriate review board for approval.

Who needs human subject research approval?

01

Researchers conducting experiments or studies involving human participants.

02

Students conducting research projects as part of their academic studies.

03

Institutions or organizations conducting research that involves human subjects.

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What is human subject research approval?

Human subject research approval is the process of obtaining permission or ethical clearance from an Institutional Review Board (IRB) to conduct research involving human participants.

Who is required to file human subject research approval?

Researchers conducting studies that involve human participants are required to file for human subject research approval.

How to fill out human subject research approval?

To fill out human subject research approval, researchers must provide detailed information about their study design, methods, potential risks to participants, and how participant confidentiality will be protected.

What is the purpose of human subject research approval?

The purpose of human subject research approval is to ensure that research involving human participants is conducted ethically and with the participants' safety and rights as the top priority.

What information must be reported on human subject research approval?

Researchers must report detailed information about the study design, methods, potential risks to participants, how participant confidentiality will be protected, and how informed consent will be obtained from participants.

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