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IORG0000108 BORG #: Institution: Louisiana State U Hath Sciences Ctr New Orleans Expires:OMB No. 09900279 Approved for use through October 31, 201807/19/2021U. S. Department of Health and Human Services
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How to fill out when is an irb

01
Start by obtaining an IRB application form from the relevant institution or organization.
02
Fill out the basic information section, including your name, contact details, and professional affiliation.
03
Provide a clear and concise description of your research project, including its objective, methodology, and potential risks or benefits to participants.
04
Outline your data collection procedures, including how you will obtain informed consent from participants and maintain their confidentiality.
05
Describe how you will recruit participants for your study, ensuring that your selection process is fair and ethical.
06
Discuss any potential conflicts of interest and how you plan to mitigate them.
07
Provide details of the qualifications and expertise of the individuals who will be involved in the research project.
08
Include any supporting documents, such as consent forms, interview questionnaires, or survey instruments.
09
Submit the completed IRB application along with all necessary documents to the designated review board.
10
Await feedback and follow any additional instructions or requests for revisions from the IRB.
11
Once your application is approved, you can proceed with your research while adhering to the guidelines set forth by the IRB.

Who needs when is an irb?

01
Researchers conducting studies involving human subjects are typically required to obtain IRB approval.
02
This includes researchers in fields such as medicine, psychology, sociology, anthropology, and education.
03
Students conducting research as part of their academic coursework or thesis may also need IRB approval.
04
Institutional and organizational review boards may have specific guidelines and criteria for determining who needs IRB approval.
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An 'IRB' refers to an Institutional Review Board, which is a committee established to review and approve research involving human subjects to ensure that ethical standards are upheld.
Researchers or institutions conducting studies involving human participants must file with the IRB to seek approval before commencing their research.
To fill out an IRB application, researchers need to provide detailed information about the research project, including study objectives, methodology, participant recruitment strategies, informed consent processes, and measures for protecting participant confidentiality.
The purpose of an IRB is to protect the rights and welfare of human research subjects by ensuring that research proposals adhere to ethical standards and federal regulations.
Researchers must report information including study title, investigator details, purpose of the study, participant demographics, risk assessment, informed consent process, and data management plans.
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