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This form is used to initiate a research project by ensuring it qualifies for expedited review by the Institutional Review Board (IRB), outlining the categories that qualify for such review alongside
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How to fill out INDIANA UNIVERSITY EAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW EXPEDITED RESEARCH CHECKLIST

01
Begin by downloading the Indiana University East IRB Expedited Research Checklist from the official website.
02
Read the instructions provided in the document thoroughly.
03
Fill out the title of your research project in the designated section.
04
Provide a brief summary of your research, including purpose, methodology, and expected outcomes.
05
Identify the population involved in your research and explain how you will recruit participants.
06
Detail the procedures you will use to collect data.
07
Specify any potential risks to participants and how you plan to minimize them.
08
Explain how you will ensure confidentiality and anonymity of the participants.
09
Include information on informed consent, detailing how you will obtain it.
10
Review your checklist for completeness and accuracy before submission.

Who needs INDIANA UNIVERSITY EAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW EXPEDITED RESEARCH CHECKLIST?

01
Researchers at Indiana University East conducting studies involving human subjects that qualify for expedited review.
02
Faculty and students who are undertaking projects requiring ethical oversight.
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People Also Ask about

In order to qualify for review via expedited procedures, the research must not be greater than minimal risk and fall into at least one of the expedited categories defined by the federal regulations.
The expedited review procedure may not be used where the identification of the subjects and/or their responses would reasonably place them at risk of criminal or civil liability, damage the subjects' financial standing, employability, insurability, reputation, or stigmatize them unless reasonable and appropriate
Detention Review Hearings SectionTime LImits 16(1) & 17(1) & 26(b) & 32(2) & 45(4) & 46(4) Five days before the hearing 31(2) Seven days after mailed 39(3) & 40(3) Five days and three days, respectively. 47(4) Ten days6 more rows • Aug 2, 2024
Projected wait times are approximately 24 months for refugee claims and 12 months for refugee appeals.
Expedited Eligibility Approved expedited protocols may be approved for a 1-year or 3-year approval period. (See Section I below.) C. Additionally, the standard requirements for informed consent (or its waiver or alteration) apply to all IRB approvals regardless of the type of review - expedited or full Committee.
The 75th percentile data, which is how long the IRB takes to finalize the review of 75% of all submissions by type of review are also calculated for each quarter. For the first quarter of 2025 the results are: 76 days for full-board, 12 days for expedited, 81 days for ceded reviews, and 19 days for exempt reviews.

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The INDIANA UNIVERSITY EAST INSTITUTIONAL REVIEW BOARD (IRB) REVIEW EXPEDITED RESEARCH CHECKLIST is a tool used to evaluate research proposals that qualify for expedited review under the regulations for human subjects research. It helps streamline the review process for studies that pose minimal risk to participants.
Researchers affiliated with Indiana University East who are conducting studies that involve human subjects and meet the criteria for expedited review must file the INDIANA UNIVERSITY EAST IRB REVIEW EXPEDITED RESEARCH CHECKLIST.
To fill out the INDIANA UNIVERSITY EAST IRB REVIEW EXPEDITED RESEARCH CHECKLIST, researchers should carefully follow the provided guidelines, ensuring that all relevant sections are completed, including study details, participant information, and risk assessments.
The purpose of the INDIANA UNIVERSITY EAST IRB REVIEW EXPEDITED RESEARCH CHECKLIST is to facilitate a thorough yet efficient review process for research proposals that involve minimal risk to participants, ensuring ethical standards and compliance with federal regulations.
The INDIANA UNIVERSITY EAST IRB REVIEW EXPEDITED RESEARCH CHECKLIST must report details such as the research title, objectives, methodology, participant recruitment processes, informed consent procedures, potential risks, and how data confidentiality will be maintained.
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