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All research involving human participants conducted by Rowan University faculty and staff is subject to IRB review. For more guidelines on exemption see the FAQ on the Rowan IRB website or the more detailed explanations in the Rowan IRB policy or the Website of the U.S. Department of Health and Human Service Office for Human Research Protections OHRP. Rowan.edu/open/provost/research/Integrityandcompliance/Irb/Irb. htm Research Exemptions Federal ...
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How to fill out rowan irb form

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How to fill out Rowan IRB form:

01
Start by downloading the Rowan IRB form from the official website.
02
Fill out the required personal information section, including your name, contact information, and affiliation with Rowan University.
03
Provide a clear and concise description of your research project in the designated section.
04
Indicate the target population and any potential risks or benefits associated with the study.
05
Include information about the research methodology, data collection procedures, and data analysis techniques.
06
If applicable, provide details about any funding or grants obtained for the research.
07
Include a comprehensive list of references that support the research proposal.
08
Review the completed form to ensure all sections are filled out accurately and completely.
09
Save a copy of the form for your records and submit it to the appropriate Rowan IRB office.

Who needs Rowan IRB form?

01
Researchers affiliated with Rowan University who are conducting human subjects research.
02
Students or faculty members who are involved in research activities that require ethical review and approval.
03
Any individual or group planning to conduct research involving human subjects within the jurisdiction of Rowan University's IRB policies and procedures.
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The Rowan IRB form is a document used to request approval for research involving human subjects at Rowan University.
Researchers who plan to conduct studies involving human subjects at Rowan University are required to file the Rowan IRB form.
To fill out the Rowan IRB form, researchers need to provide detailed information about the research protocol, study participants, risks and benefits, informed consent process, and safeguarding of participants' rights and confidentiality.
The purpose of the Rowan IRB form is to ensure that research involving human subjects follows ethical guidelines and protects the rights and well-being of the participants.
The Rowan IRB form requires researchers to report information such as the purpose of the study, risks and benefits to participants, recruitment methods, data collection procedures, informed consent process, safeguards for privacy and confidentiality, and potential conflicts of interest.
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