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This document provides an application for expedited IRB review for the Pennsylvania Cancer Alliance's bioinformatics project, outlining objectives, significance, methodologies, and human subject considerations.
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How to fill out application for expedited irb

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How to fill out APPLICATION FOR EXPEDITED IRB REVIEW

01
Obtain the Application for Expedited IRB Review form from the IRB office or website.
02
Read the instructions carefully to understand the eligibility criteria for expedited review.
03
Fill out the project title, principal investigator's details, and contact information at the top of the form.
04
Provide a brief summary of the research project, including objectives and methodology.
05
Justify why the study qualifies for expedited review by referencing the appropriate federal categories.
06
Describe the participant recruitment process and include details about the informed consent process.
07
Address any potential risks to participants and outline the plans for minimizing these risks.
08
Include any necessary supporting documents, such as consent forms or questionnaires.
09
Review the application for completeness and accuracy before submission.
10
Submit the application to the IRB for review along with any required fees or additional documents.

Who needs APPLICATION FOR EXPEDITED IRB REVIEW?

01
Researchers conducting studies that qualify for expedited review.
02
Faculty members involved in research requiring IRB oversight.
03
Students conducting research as part of their academic programs.
04
Any institution or organization that will be conducting research involving human subjects.
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The APPLICATION FOR EXPEDITED IRB REVIEW is a formal request submitted to an Institutional Review Board (IRB) to seek expedited approval for research studies that involve minimal risk to participants.
Researchers or investigators conducting studies that qualify for expedited review, typically those involving minimal risk, are required to file the APPLICATION FOR EXPEDITED IRB REVIEW.
To fill out the APPLICATION FOR EXPEDITED IRB REVIEW, researchers should provide detailed information about the study, including the research protocol, objectives, participant selection criteria, informed consent process, and any potential risks involved.
The purpose of the APPLICATION FOR EXPEDITED IRB REVIEW is to ensure the protection of human subjects involved in research by providing a streamlined process for studies that present minimal risk.
The APPLICATION FOR EXPEDITED IRB REVIEW must report information including the study title, principal investigator details, study objectives, methodology, participant demographics, informed consent procedures, and any potential risks or benefits.
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