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INSTITUTIONAL REVIEW BOARD APPLICATION EXPEDITED REVIEW For research involving the use of EXISTING and CONFIDENTIAL data, records, or specimens This application has been created specifically for retrospective
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How to fill out irb expedited review existing

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How to fill out IRB expedited review existing:

01
Review the IRB expedited review application form provided by your institution or organization. Familiarize yourself with the sections and questions that need to be addressed.
02
Gather all relevant documents and information required for the expedited review process. This may include study protocols, informed consent forms, research instruments, and any supporting documents.
03
Begin by providing a clear and concise title for your research study. This should accurately reflect the purpose of your research.
04
Describe the background and rationale of your study. Explain why the research is being conducted and the significance of the proposed research question.
05
Clearly articulate the research objectives and hypotheses of your study. State what you intend to investigate and any specific research questions you aim to answer.
06
Detail the study design and methods you will be using. Explain the procedures, recruitment process, data collection methods, and any interventions or treatments that will be implemented.
07
Address any risks and benefits associated with the study. Discuss potential harm to participants and how these risks will be minimized. Also, outline any potential benefits that may result from your research.
08
Include an informed consent process which outlines how you will obtain informed consent from participants and ensure their understanding of the study procedures.
09
Outline the data management plan and how confidentiality will be maintained. Describe how data will be collected, stored, and analyzed.
10
Finally, include any additional information or documentation that may be requested in the expedited review process. This may include CVs of key personnel, funding sources, and any other supporting documents required by the IRB.

Who needs IRB expedited review existing:

01
Researchers who are conducting studies that fall under the categories eligible for expedited review. Expedited review is typically given to research that poses minimal risk to participants and meets specific criteria outlined by the IRB.
02
Studies that involve minimal interventions, such as surveys, interviews, or analysis of existing data, may qualify for expedited review.
03
Researchers who need a faster review process and do not require the oversight and approval of the full IRB board. This may be due to time constraints or the urgency of the research.
04
Researchers who have already submitted an initial IRB application and require a review of modifications or amendments to their study protocol.
05
Depending on institutional policies and guidelines, undergraduate and graduate students, faculty members, and outside researchers may all require IRB expedited review for their research projects.
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IRB expedited review is a streamlined review process for research studies that pose minimal risk to participants.
Researchers conducting studies that fall under the minimal risk category are required to file for IRB expedited review.
To fill out an IRB expedited review, researchers need to provide detailed information about the study design, procedures, risks, and informed consent process.
The purpose of IRB expedited review is to ensure the protection of human subjects in research while expediting the review process for studies with minimal risk.
Researchers must report details about the study protocol, informed consent process, risks to participants, and any potential conflicts of interest.
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