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EXEMPT PROTOCOL APPLICATION Exempt CategoriesWhiletheOfficeofSponsoredProgramsand/ortheIRBisultimatelyresponsiblefordecidingifresearch qualifiesforexemption, investigatorsareaskedtomakeaninitialdeterminationoftheappropriateexemption category.
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How to fill out institutional review board

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Step 1: Obtain the necessary forms and documents from the institutional review board (IRB) office.
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Step 2: Read and understand the instructions provided with the forms.
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Step 3: Fill out the required information in the application form, including project title, investigator details, study objectives, methodology, and participant recruitment procedures.
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Step 4: Attach any supporting documents or materials requested by the IRB, such as informed consent forms, research protocols, and data collection instruments.
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Step 5: Review the completed application for accuracy and completeness.
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Step 6: Submit the application along with all the required documents to the IRB office.
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Step 7: Wait for the IRB review and approval process to be completed.
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Step 8: Address any concerns or requested modifications from the IRB, if applicable.
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Step 9: Once approved, begin the research study while ensuring compliance with the IRB policies and guidelines.
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Step 10: Report any adverse events or unexpected findings to the IRB as required.
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Step 11: Follow any post-approval procedures outlined by the IRB, such as annual reporting or study progress updates.

Who needs institutional review board?

01
Researchers who conduct studies involving human participants.
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Academic institutions conducting research.
03
Government agencies conducting research projects.
04
Medical professionals conducting clinical trials.
05
Pharmaceutical companies seeking approval for new drugs.
06
Organizations conducting social science research.
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Any individual or entity that plans to conduct research that involves human subjects and seeks to ensure ethical standards and participant rights are protected.
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An Institutional Review Board (IRB) is a committee established to review and approve research involving human subjects, ensuring that their rights, welfare, and privacy are protected.
Researchers conducting studies involving human subjects, including faculty, students, and staff at institutions that receive federal funding or are affiliated with research organizations, are required to file with an Institutional Review Board.
To fill out an IRB application, researchers must provide detailed information about the study design, purpose, methodology, potential risks and benefits to participants, and plans for data management and confidentiality.
The purpose of an Institutional Review Board is to protect the rights and welfare of human research participants by reviewing research proposals to ensure ethical standards are met.
Researchers must report information including study objectives, methodology, participant recruitment strategies, informed consent processes, potential risks and benefits, and plans for data analysis and confidentiality.
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