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Template Version 2019OFFICE OF RESEARCHNSUNSU Institutional Review Board/Ethics Review CommitteeReview of a New Proposal Involving Human Subjects ResearchPrimary Reviewer Template (see instructions on page three)IRB/ERC Review Code: 2019/OR
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How to fill out irb primary reviewer templatedocx
How to fill out irb primary reviewer templatedocx
01
Open the IRB primary reviewer template document in a word processing software.
02
Fill in the required information such as title, date, study number, principal investigator, and contact information.
03
Provide detailed information on the study design, purpose, procedures, and risks involved.
04
Include the justification for the study and any potential benefits to research participants.
05
Make sure to review and revise the document for accuracy and completeness before submitting it for review.
Who needs irb primary reviewer templatedocx?
01
Researchers conducting studies that require review and approval by an Institutional Review Board (IRB) need the IRB primary reviewer template document to submit their research protocols for evaluation.
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What is irb primary reviewer templatedocx?
IRB primary reviewer templatedocx is a document template used for reviewing research projects involving human subjects.
Who is required to file irb primary reviewer templatedocx?
Researchers or institutions conducting research involving human subjects are required to file the irb primary reviewer templatedocx.
How to fill out irb primary reviewer templatedocx?
IRB primary reviewer templatedocx should be filled out by providing detailed information about the research project, including protocols for human subject protection and consent procedures.
What is the purpose of irb primary reviewer templatedocx?
The purpose of irb primary reviewer templatedocx is to ensure that research projects involving human subjects comply with ethical standards and regulations.
What information must be reported on irb primary reviewer templatedocx?
Information such as the research protocol, risks and benefits to human subjects, consent procedures, and data handling protocols must be reported on irb primary reviewer templatedocx.
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