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Revised 10/17/2013 Claremont Graduate University Institutional Review Board (IRB) Application for Research Project Review LEAVE BLANKER IRB USE ONLY. IRB NUMBER & DATE RECEIVED: Action Taken: Exempt

How to fill out cgu irb form

How to fill out CGU IRB?

1. Begin by carefully reading the instructions and guidelines provided by CGU (Claremont Graduate University) for filling out the IRB (Institutional Review Board) application. Familiarize yourself with the purpose of the IRB and its requirements.
2. Prepare all the necessary documents and information that will be needed to complete the CGU IRB application. This may include details about the research project, informed consent forms, participant recruitment materials, questionnaire or interview scripts, and any other relevant supporting documents.
3. Start filling out the CGU IRB application form, paying close attention to each section. Provide accurate and concise information about your research project, including its objectives, methodology, and potential risks or benefits for participants.
4. Specify the target population and describe the sample size you will be working with. Explain how you plan to recruit participants, ensuring that your methods are ethical and respectful.
5. Address any potential ethical issues that your research may encounter and explain how you plan to minimize or mitigate them. This may include measures to protect participant confidentiality, obtaining informed consent, and ensuring the safety and well-being of participants.
6. Complete the sections of the CGU IRB application that ask for information about your background, qualifications, and affiliations. Provide accurate and up-to-date details to establish your credibility as a researcher.
7. Review the completed CGU IRB application for any errors or inconsistencies. Make sure that all the required sections have been filled out, and double-check the accuracy of the information provided.
8. Once you are satisfied with the application, submit it to the CGU IRB office through their designated submission process. Follow any additional instructions provided by CGU regarding the submission, such as including copies of supporting documents or signature requirements.

Who needs CGU IRB?

1. Researchers conducting human subjects research within Claremont Graduate University (CGU) or affiliated with CGU are required to obtain IRB approval. This includes faculty members, graduate students, and other individuals involved in research activities involving human participants.
2. CGU IRB is particularly necessary for projects that involve interventions, surveys, interviews, experiments, or studies that collect data directly from human participants. It is essential to ensure the protection of individuals' rights, welfare, and privacy during the research process.
3. While CGU IRB primarily focuses on research conducted within the university community, researchers from external organizations or institutions collaborating with CGU may also be required to seek CGU IRB approval if their research involves CGU faculty, students, or facilities.

Note: It is important to consult CGU's specific guidelines and requirements regarding the application process and who precisely needs CGU IRB approval, as policies may slightly vary.

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What is cgu irb?

CGU IRB stands for Claremont Graduate University Institutional Review Board, it is responsible for reviewing and approving research involving human subjects.

Who is required to file cgu irb?

All researchers at Claremont Graduate University who are conducting research involving human subjects are required to file CGU IRB.

How to fill out cgu irb?

Researchers can fill out CGU IRB by submitting an application form, protocol, and any other required documents to the IRB office.

What is the purpose of cgu irb?

The purpose of CGU IRB is to protect the rights and welfare of human subjects participating in research conducted by the university.

What information must be reported on cgu irb?

Researchers must report information about their study design, potential risks to participants, informed consent process, and data handling procedures.