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For IRB Use Only Log Number Date Received Minersville University of Pennsylvania Institutional Review Board for the Protection of Human Subjects Request for IRB Protocol Number for Pending Research
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How to fill out for irb use only

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How to fill out for irb use only:

01
Begin by providing the necessary information in the designated fields. This may include the project title, research team members, and the IRB protocol number.
02
Clearly identify the sections of the form that are intended for "IRB use only." These sections may be marked as such or may have a specific heading indicating that the information provided will only be accessed by the IRB. Ensure that you only add relevant information to these sections.
03
Double-check all the information you have entered to ensure accuracy. This is particularly important for any sensitive or confidential data that may be included in the form.
04
Follow any additional instructions or requirements specified by your institution's IRB guidelines. This may include attaching supporting documents, obtaining necessary signatures, or providing additional explanations.
05
Once you have completed all the relevant sections, review the form one final time to ensure there are no errors or omissions. Take note of any special submission instructions, deadlines, or contact information provided by your IRB.

Who needs for irb use only:

01
Researchers and research institutions who are submitting a study for review to the Institutional Review Board (IRB) may need to fill out the "IRB use only" sections of the form.
02
The purpose of these sections is to provide the IRB members with any additional information, clarifications, or documentation that is necessary for them to conduct their review.
03
Access to the information in the "IRB use only" sections is typically limited to the designated IRB members, who are responsible for reviewing and approving research protocols to ensure compliance with ethical guidelines, regulatory requirements, and the protection of human subjects.
04
Researchers and research institutions are required to fill out the "IRB use only" sections accurately and comprehensively to facilitate a thorough review process and to provide the necessary information for the IRB members to make an informed decision regarding the research study.
05
Failure to complete the "IRB use only" sections or providing incomplete or inaccurate information may result in delays in the review process or even the rejection of the research protocol. It is important to carefully follow the instructions and guidelines provided by the IRB to ensure a successful submission.
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For irb use only refers to information that is restricted and can only be accessed by the Institutional Review Board.
Researchers and individuals conducting studies involving human subjects are required to file for irb use only.
The for irb use only form must be filled out accurately and completely, providing all relevant information about the research study.
The purpose of for irb use only is to protect the confidentiality and privacy of human subjects involved in research studies.
Information such as personal data, medical records, and any other sensitive information related to human subjects must be reported on for irb use only.
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