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The Catholic University of AmericaInstitutional Review Board for the Protection Of Human SubjectsRequest to Renew an Approved Protocol (no changes)Please complete this form and return it to: Office
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Step 1: Start by gathering all the necessary documents and information related to the study or research project that requires the review.
02
Step 2: Review the guidelines and regulations provided by your institution or the relevant governing body to ensure compliance with all requirements.
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Step 3: Prepare a detailed research protocol, including the study objectives, methodology, participant selection criteria, data collection methods, and analysis plan.
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Step 4: Obtain informed consent forms or necessary documentation for obtaining informed consent from participants.
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Step 5: Submit the completed Institutional Review Board (IRB) application form along with all the supporting documents to the designated authority.
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Step 6: Await the review process, which may involve a preliminary assessment, additional documentation requests, and revisions.
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Step 7: Address any concerns or queries raised by the IRB committee promptly and make any required amendments to the application or research protocol.
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Step 8: Once the review is complete and all necessary changes are made, obtain the final approval from the IRB committee.
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Step 9: Adhere to the approved research protocol and comply with any reporting requirements specified by the IRB committee.
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Step 10: Continuously ensure ongoing compliance with IRB guidelines and regulations throughout the course of the research or study.

Who needs institutional review boardcommittee for?

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Researchers and scientists planning to conduct studies involving human participants.
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Academic institutions and universities undertaking research projects.
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Medical professionals and healthcare organizations involved in clinical trials.
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Government agencies and regulatory bodies overseeing research in fields like psychology, sociology, or healthcare.
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Any individual or organization conducting research that involves human subjects and aims to ensure ethical and responsible treatment of participants.

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An Institutional Review Board (IRB) committee is responsible for reviewing and overseeing research involving human subjects to ensure ethical standards are met and participants' rights are protected.
Researchers conducting studies involving human subjects, affiliated with institutions that receive federal funding or are engaged in certain types of clinical research are required to file with an IRB.
To fill out an IRB application, researchers must provide detailed information about the research project, including the study purpose, methodology, informed consent process, and measures to ensure participant confidentiality.
The purpose of an IRB is to protect the rights and welfare of human research participants by reviewing research proposals and ensuring compliance with ethical standards and regulations.
Researchers must report information including study objectives, research design, participant recruitment methods, informed consent process, and potential risks and benefits to participants.
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