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IRB Guidelines 1.3 Institutional Review Board (IRB) HIPAA Research Implications Version 1.1: Created 4/20/2016 Overview The Health Insurance Portability and Accountability Act of 1996 (HIPAA) and

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How to fill out ung irb form

Point by point, here is how to fill out the UNG IRB form:

01

Start by carefully reading the instructions provided with the UNG IRB form. This will give you a clear understanding of the requirements and procedures involved in completing the form.

02

Gather all the necessary information and documentation before beginning to fill out the form. This may include details about the research project, the purpose of the study, ethical considerations, and any potential risks or benefits associated with the research.

03

Begin filling out the form by providing your personal information, such as your name, contact details, and affiliation with the university or institution conducting the research.

04

Clearly state the title of your research project and provide a brief description of the study. This should include the objectives and methodology you plan to employ.

05

Indicate whether your study involves human subjects or not. If it does, explain how you will recruit participants, ensure their informed consent, and protect their privacy and confidentiality.

06

Describe the potential risks, if any, associated with your research. This may include physical, psychological, or social risks that participants might encounter during the study. It is important to outline any measures in place to minimize or mitigate these risks.

07

Outline the benefits that may result from your research. These could include advancements in knowledge, potential applications, or improvements in the field of study.

08

Specify any resources or external approvals required to conduct the research. This might include access to certain facilities, funding, or collaboration with other institutions or individuals.

09

Lastly, sign and date the form to indicate your consent and agreement with the information provided.

Who needs the UNG IRB?

The UNG IRB is typically required by researchers and individuals planning to conduct research projects involving human subjects. This includes faculty members, students, and other affiliated researchers within the University of North Georgia or any collaborating institutions. The UNG IRB ensures that the research is conducted ethically and in compliance with applicable regulations to protect the rights and welfare of the research participants.

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What is ung irb?

Ung irb stands for Undergraduate Institutional Review Board, which is a committee that reviews and approves research involving human subjects conducted by undergraduate students.

Who is required to file ung irb?

Undergraduate students conducting research involving human subjects are required to file ung irb.

How to fill out ung irb?

To fill out ung irb, undergraduate students need to provide information about their research project, including the study design, risks and benefits to participants, and consent forms.

What is the purpose of ung irb?

The purpose of ung irb is to ensure that research involving human subjects conducted by undergraduate students is ethical and protects the rights and welfare of participants.

What information must be reported on ung irb?

Information such as study design, informed consent process, risks and benefits to participants, and procedures for ensuring confidentiality must be reported on ung irb.

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