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IRB Members Handbook P a g e 38 Health Insurance Portability and Accountability Act (HIPAA) The Health Insurance Portability and Accountability Act (HIPAA), also referred to as the Privacy Rule, at

How to fill out etsu irb form

How to fill out ETSU IRB:

1. Obtain the necessary forms from the ETSU IRB website. These forms typically include an application form, consent form templates, and any additional documentation required for your specific research study.
2. Read the instructions carefully and familiarize yourself with the guidelines and regulations set forth by the ETSU IRB. It is important to understand the ethical considerations and requirements for conducting research involving human subjects.
3. Complete the application form with accurate and detailed information about your research study. Provide a clear and concise description of the study objectives, methods, and any potential risks or benefits to participants. Include any supporting documents or materials requested by the ETSU IRB.
4. Develop the consent forms for your study participants using the provided templates or following the ETSU IRB guidelines. These forms should outline the purpose of the study, the procedures involved, any potential risks or benefits, and the voluntary nature of participation. Ensure that the language used is easily understood by your target population.
5. Submit your completed application and consent forms to the ETSU IRB for review. Pay attention to any specific submission deadlines and requirements specified by the IRB. Include any additional supporting documentation or materials as requested.
6. Respond promptly to any clarification or revision requests from the ETSU IRB. It is common for the IRB to request modifications or additional information to ensure compliance with ethical guidelines. Make any necessary changes to your study design or consent forms based on their feedback.
7. If your research study involves vulnerable populations or poses potential risks, you may need to attend an IRB committee meeting to present and discuss your study. Respond to any questions or concerns raised by the committee members and provide further clarification if needed.
8. Once your study has received final approval from the ETSU IRB, you can proceed with conducting your research. Ensure that you follow the approved protocol and adhere to any ongoing reporting requirements or modifications requested by the IRB.

Who needs ETSU IRB:

1. Researchers conducting research involving human subjects within the jurisdiction of East Tennessee State University (ETSU) need ETSU IRB approval. This includes faculty, staff, students, and external researchers collaborating with ETSU.
2. Any individuals or organizations conducting research funded or supported by ETSU or utilizing ETSU facilities or resources are also required to obtain ETSU IRB approval.
3. The ETSU IRB is responsible for ensuring the ethical treatment of human subjects in research and the protection of their rights and welfare. Therefore, any researcher conducting research involving human subjects must comply with the IRB's review and approval process.

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What is etsu irb?

The ETSU IRB stands for East Tennessee State University Institutional Review Board, which is responsible for reviewing and approving research involving human subjects.

Who is required to file etsu irb?

Researchers and institutions conducting research involving human subjects are required to file ETSU IRB.

How to fill out etsu irb?

To fill out ETSU IRB, researchers must submit a research protocol detailing the study design, methods, risks, and benefits to human subjects.

What is the purpose of etsu irb?

The purpose of ETSU IRB is to protect the rights and welfare of human subjects participating in research studies.

What information must be reported on etsu irb?

Researchers must report details of the study design, recruitment methods, informed consent process, risks to participants, and data management on ETSU IRB.