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IRB Reviewer Form for Pregnant Women, Fetuses, Neonates (Appendix K)If this research has requested the inclusion of participants who are pregnant, fetuses, or neonates (of uncertain viability and
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The IRB reviewer form is a document used to evaluate research proposals involving human subjects to ensure they meet ethical standards and comply with regulatory requirements.
Researchers and institutions conducting studies involving human subjects are required to file the IRB reviewer form.
To fill out the IRB reviewer form, provide detailed information about the research study, including the study's objectives, methodology, potential risks and benefits, and how participants' rights will be protected.
The purpose of the IRB reviewer form is to ensure that all research involving human subjects is ethically conducted, safeguarding participants' rights and well-being.
The information that must be reported on the IRB reviewer form includes study title, principal investigator details, study objectives, participant recruitment methods, consent process, and risk assessment.
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