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This document outlines the procedures and requirements for submitting a Full Review Certification application for research involving human subjects at KSU, ensuring compliance with federal regulations
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How to fill out irb full review certification

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How to fill out IRB Full Review Certification Request Procedures and Application

01
Gather all necessary documents and information required for the IRB Full Review.
02
Complete the IRB Full Review Certification Request form with accurate details.
03
Provide a detailed description of the research project, including objectives, methodology, and potential risks.
04
Attach any supplementary materials, such as informed consent forms, recruitment materials, and data collection instruments.
05
Review the completed application for completeness and accuracy.
06
Submit the application to the IRB office via the specified submission method (online portal, email, etc.).
07
Keep a copy of the submitted application for your records.

Who needs IRB Full Review Certification Request Procedures and Application?

01
Researchers conducting clinical trials or any study involving human subjects.
02
Faculty members at academic institutions involved in research.
03
Students conducting research as part of their academic programs.
04
Organizations planning to undertake studies involving human participants that require ethical approval.
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IRB Process Submission of Research Proposal: Researchers submit their research proposal to the IRB. Initial Review: Exemption Determination (if applicable): Expedited Review (if applicable): Full Board Review (if applicable): Approval Decision: Ongoing Oversight:
The first step of the process is to plan the research project involving human participants or subjects. This needs to be well conceptualized before the process can go forward. If it is a student project, a faculty advisor must be included for consultation in the development of a protocol to be submitted to the IRB.
The Code of Federal Regulations (Title 45, Part 46) and the Belmont Report (PDF) specify three basic ethical principles which must guide all human subjects research: respect for persons, beneficence and justice.
Studies that involve more than minimal risk require review at full board IRB meeting (also referred to as Convened Review). The research requires approval from a majority of those members.
Under the Common Rule, IRBs must have at least five members and include at least one scientist, one non-scientist, and “one member who is not otherwise affiliated with the institution and who is not part of the immediate family of a person who is affiliated with the institution”(§ 46.107(d)).
If your study is more than minimal risk, it will be harder for you to get IRB approval. You will need to justify why you are running the study. Less common types of risk for psychology studies are social, physical, and financial.
IRB Review Process: The IRB review process is in place to protect the rights and welfare of humans participating as subjects in research studies. IRB approval is required when research involving human subjects: Receives federal funds either directly or indirectly. Takes place at a university or hospital.

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The IRB Full Review Certification Request Procedures and Application is a formal process through which researchers submit their research proposals to the Institutional Review Board (IRB) for ethical review and approval before conducting studies involving human subjects.
All researchers, faculty, staff, and students conducting research involving human subjects at institutions that have an IRB must file the IRB Full Review Certification Request Procedures and Application.
To fill out the IRB Full Review Certification Request Procedures and Application, researchers need to provide detailed information about their research protocol, including study objectives, methodology, participant recruitment, informed consent processes, and data management plans. It often involves completing specific forms provided by the IRB.
The purpose of the IRB Full Review Certification Request Procedures and Application is to ensure that proposed research projects are assessed for ethical considerations, participant safety, and compliance with federal regulations and institutional policies.
The information required includes the research title, names of investigators, a detailed study description, potential risks and benefits to participants, consent forms, recruitment strategies, data collection methods, and plans for ensuring participant confidentiality.
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