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IRB PoliciesEffective Date: 10 May 2019Version 1.2Table of Contents HRP001POLICY: Definitions3HRP002POLICY: Abbreviations8HRP003POLICY: Designations9HRP010POLICY: Human Research Protection Program10HRP020POLICY:
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01
Familiarize yourself with the IRB policies of your university. These policies outline the ethical considerations and guidelines that researchers must follow when conducting studies involving human subjects.
02
Start by obtaining the necessary forms and documents required for submitting an IRB application. These may include consent forms, recruitment materials, and study protocols.
03
Complete the IRB application form, ensuring that all sections are filled out accurately and completely. Provide detailed information about the study design, research methods, and the potential risks and benefits for participants.
04
Prepare all supporting documentation, including informed consent forms, recruitment materials, and any necessary documents to demonstrate the qualifications and expertise of the research team.
05
Submit the completed application and supporting documents to the appropriate IRB office at your university, following any specific submission guidelines and deadlines.
06
Await review and approval of your application. The IRB will evaluate your study for ethical considerations, participant protections, and compliance with relevant regulations and policies.
07
If revisions or modifications to the study are required, make the necessary changes and resubmit the application for further review.
08
Once your study receives IRB approval, you can begin recruiting participants and conducting your research. Remember to continue adhering to the approved protocols and guidelines throughout the study.
09
Keep track of any changes or updates to your study and promptly report them to the IRB. This includes any deviations from the approved protocols, adverse events, or new insights that may impact participant safety.
10
After the completion of your study, provide a final report to the IRB, including the study outcomes, participant feedback (if applicable), and any additional documentation or records as requested.

Who needs irb policies - university?

01
Universities and academic institutions that conduct research involving human subjects need IRB policies in place.
02
These policies ensure that the rights and welfare of research participants are protected and that studies involving human subjects are conducted ethically and in compliance with relevant regulations.
03
Researchers, faculty members, students, and other individuals affiliated with the university who plan to conduct research involving human subjects must adhere to the university's IRB policies.
04
These policies may also apply to non-faculty researchers, visiting scholars, and collaborators who are involved in research projects conducted at the university.
05
Furthermore, funding agencies and grant providers often require researchers to have IRB approval and to follow specific policies when conducting studies.
06
By implementing IRB policies, universities demonstrate their commitment to upholding ethical standards in research and ensuring the protection of human subjects.
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IRB policies at a university are guidelines and procedures established by the Institutional Review Board to ensure ethical standards are met when conducting research involving human subjects.
Researchers, faculty, and students conducting research involving human subjects at a university are required to file IRB policies with the Institutional Review Board.
To fill out IRB policies at a university, researchers need to provide detailed information about their research project, including the purpose, methods, risks, and potential benefits to participants.
The purpose of IRB policies at a university is to protect the rights and welfare of human subjects participating in research studies, ensuring that ethical standards are followed.
IRB policies at a university typically require researchers to report information such as the consent process, confidentiality measures, data management procedures, and risk assessment.
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