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INTER AMERICAN UNIVERSITY OF PUERTO RICO INSTITUTIONAL REVIEW BOARD (IRB) APPLICATION FOR PROTOCOL REVIEW IAUPRIRB FORM REV 01/2019 Research Study Title:If protocol is a sponsored Project:Name of
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How to fill out application for protocol review

01
Start by reading the guidelines and requirements for the protocol review.
02
Collect all the necessary documents and information that are required to fill out the application.
03
Begin by providing your personal details such as name, contact information, and affiliation.
04
Clearly state the purpose and objectives of the protocol that needs to be reviewed.
05
Outline the methodology and procedures that will be followed in the protocol.
06
Include any potential risks or ethical considerations associated with the protocol.
07
Provide a detailed timeline for the implementation of the protocol.
08
List any resources or funding that will be needed to carry out the protocol.
09
Finally, review and proofread your application before submitting it for the protocol review.

Who needs application for protocol review?

01
Researchers and scientists who are conducting studies or experiments involving human subjects or animals typically need to submit an application for protocol review.
02
Institutions and organizations that oversee research ethics, such as universities, hospitals, or government agencies, may also require protocol review applications.
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Application for protocol review is a formal request submitted to a governing body or institutional review board seeking approval for conducting a study involving human subjects.
Researchers, scientists, or anyone planning to conduct a study involving human subjects are required to file an application for protocol review.
The application for protocol review can typically be filled out online or in a physical form provided by the governing body or institutional review board. It usually requires detailed information about the study design, procedures, and potential risks to participants.
The purpose of the application for protocol review is to ensure that studies involving human subjects are conducted ethically, following established guidelines and regulations to protect the rights and welfare of participants.
Information required on the application for protocol review may include study objectives, methodology, recruitment procedures, informed consent process, potential risks and benefits, data management plan, and qualifications of researchers.
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