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1 RESEARCH WITH HUMAN SUBJECTS INVESTIGATOR IS MANUAL UNIVERSITY OF THE PACIFIC Institutional Review Board Research & Graduate Studies Acknowledgement: The University of the Pacific IRB would like
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01
Step 1: Familiarize yourself with the guidelines and requirements set forth by your institution's Institutional Review Board (IRB).
02
Step 2: Gather all the necessary information regarding the research study, including the purpose, methods, and potential risks involved.
03
Step 3: Complete the IRB application form, providing detailed information about the study design, data collection procedures, and protection measures for human subjects.
04
Step 4: Prepare all supporting documents, such as consent forms, questionnaires, and recruitment materials, ensuring they comply with ethical standards and regulations.
05
Step 5: Submit the application and all necessary documents to the IRB office, following their designated submission process.
06
Step 6: Await the review process, which may involve revisions or additional information requests.
07
Step 7: Address any concerns or feedback provided by the IRB, making necessary modifications to your study protocol.
08
Step 8: Once the IRB approves your study, you can begin recruiting participants and conducting research while ensuring ongoing compliance with the approved protocol.
09
Step 9: Keep records of all IRB communications, approvals, and modifications for future reference and auditing purposes.

Who needs institutional review board for?

01
Researchers conducting studies involving human subjects, whether it is in the fields of medicine, social sciences, psychology, or any other discipline, typically need to seek approval from an Institutional Review Board (IRB).
02
Universities, colleges, and other educational institutions that conduct research involving human participants also require IRB oversight.
03
Government agencies, pharmaceutical companies, and organizations involved in research that affects human subjects must comply with IRB regulations.
04
Healthcare institutions, hospitals, and clinics that engage in research activities involving human participants need to seek IRB approval.
05
Non-profit organizations and private research institutions conducting studies with human subjects are also required to involve an IRB.
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The institutional review board is responsible for reviewing and approving research involving human subjects to ensure ethical guidelines are followed.
Researchers conducting studies involving human subjects are required to file an institutional review board.
To fill out an institutional review board, researchers must provide detailed information about the study protocol, potential risks to participants, and how participant confidentiality will be maintained.
The purpose of an institutional review board is to protect the rights and welfare of human research subjects.
The institutional review board must include information on the study design, recruitment process, informed consent procedures, and risk assessment.
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