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Get the free eIRB Department Reviewer Quick Reference - umdnj

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A guide for department reviewers on how to navigate the eIRB system, access their personal workspace, view and edit notes, issue approvals, and upload documents related to study submissions.
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How to fill out eIRB Department Reviewer Quick Reference

01
Log in to the eIRB system using your credentials.
02
Navigate to the section labeled 'Department Reviewer Quick Reference'.
03
Download or open the provided form for filling out the Quick Reference.
04
Fill in the required fields, including the study title, principal investigator, and department information.
05
Review the checklist items to ensure all necessary components are addressed.
06
Provide any additional notes or comments as needed for clarity.
07
Save the completed document and submit it as per the institution's guidelines.

Who needs eIRB Department Reviewer Quick Reference?

01
Department reviewers involved in the eIRB process.
02
Principal investigators seeking guidance on submission requirements.
03
Administrative staff assisting in the review process.
04
Institutional Review Board (IRB) members for reference during evaluations.
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The eIRB Department Reviewer Quick Reference is a guide designed to assist department reviewers in navigating and utilizing the electronic Institutional Review Board (eIRB) system effectively.
Department reviewers assigned to evaluate research proposals involving human subjects are required to utilize the eIRB Department Reviewer Quick Reference.
To fill out the eIRB Department Reviewer Quick Reference, reviewers should follow the step-by-step instructions provided in the guide, ensuring all necessary sections are completed and the information accurately reflects the research proposal being reviewed.
The purpose of the eIRB Department Reviewer Quick Reference is to streamline the review process, ensuring that department reviewers have clear guidelines and essential information needed to assess research proposals effectively.
The eIRB Department Reviewer Quick Reference must report essential information such as the study title, principal investigator, summary of the research proposal, assessment of risks and benefits, and any recommendations or required modifications.
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