Get the free UNC 's IRB Authorization Agreement (IAA) template - UNC Research

2. 11. Maintains responsibility for reporting any COI or/ FCOIs as required by applicable funding or regulatory agencies. 6. Report determinations of Serious Noncompliance Continuing Noncompliance an Unanticipated Problem Involving Risks to Subjects or Others a Suspension of IRB Approval or a Termination of IRB Approval to OHRP FDA or any other applicable agency as required under applicable rules or regulations. 2. 1. Comply with the terms of this Agreement and the terms of Relying...

How to fill out unc s irb authorization

How to fill out unc s irb authorization

1. Ensure that you have the necessary research materials, protocols, and documents required to fill out the UNC S IRB authorization form.
2. Read the instructions provided on the form carefully to understand the information and details you need to provide.
3. Start filling out the form by entering your personal information such as name, contact details, and affiliation with the University.
4. Provide a clear and concise title for your research project.
5. Describe the purpose of your research and provide an overview of the methodology you plan to follow.
6. Indicate the target population or sample you will be working with and justify your selection.
7. Explain the potential risks and benefits associated with your research and how you plan to mitigate any risks.
8. Include any measures you will take to maintain participant confidentiality and privacy.
9. Fill out any additional sections or questions on the form as instructed, ensuring that all necessary information is provided.
10. Review the completed form for accuracy and completeness.
11. Submit the filled-out UNC S IRB authorization form to the relevant authority or IRB committee for review.
12. Wait for the approval or feedback from the IRB committee before proceeding with your research.

Who needs unc s irb authorization?

1. Anyone conducting research involving human participants at the University of North Carolina (UNC) requires UNC S IRB authorization.
2. This includes students, faculty members, researchers, and staff who are involved in research projects that involve human subjects.
3. The authorization ensures that ethical guidelines and participant welfare are upheld during the research process.

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What is unc s irb authorization?

UNC S IRB authorization is the approval granted by the University of North Carolina's Institutional Review Board for a research study involving human subjects.

Who is required to file unc s irb authorization?

Researchers and investigators conducting studies involving human subjects at the University of North Carolina are required to file UNC S IRB authorization.

How to fill out unc s irb authorization?

UNC S IRB authorization can be filled out online through the IRB portal provided by the University of North Carolina.

What is the purpose of unc s irb authorization?

The purpose of UNC S IRB authorization is to ensure that research involving human subjects is conducted ethically and in compliance with regulations to protect the rights and welfare of the participants.

What information must be reported on unc s irb authorization?

UNC S IRB authorization requires information such as study protocols, informed consent forms, risks and benefits to participants, and procedures for protecting participant confidentiality.