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This document is intended for researchers at Southern University - Baton Rouge to report the status and details of their approved research projects to the Institutional Review Board (IRB), including
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How to fill out Summary or Annual Report for Non-Exempt Research

01
Gather all relevant research data and findings from the reporting period.
02
Ensure that all team members have contributed their sections or findings for accuracy.
03
Format the report according to the guidelines provided by the funding agency or organization.
04
Write a clear summary of the research objectives and outcomes in the introduction.
05
Include sections for methodology, results, and discussions in a structured manner.
06
Use tables, figures, and charts to visually present data where appropriate.
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Check for compliance with any ethical or regulatory requirements in your section.
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Review the entire report for grammar, clarity, and consistency.
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Submit the report by the deadline, ensuring you have followed all submission instructions.

Who needs Summary or Annual Report for Non-Exempt Research?

01
Researchers conducting non-exempt studies funded by government or private agencies.
02
Institutions that oversee research compliance and funding administration.
03
Ethics review boards that require oversight of research activities.
04
Funding agencies that need reports to assess the impact and compliance of their investments.
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People Also Ask about

Some examples of Exempt research are: surveys or interviews. benign behavioral interventions. passive observation of public behavior without collection of identifiers.
Although studies that qualify for exempt status do not have the same federal requirements for research involving human subjects as non-exempt studies, investigators still have a responsibility to protect the rights and welfare of their subjects, adhere to UCB policies, and conduct their research in ance with the
“Exempt” human subjects research is a sub-set of research involving human subjects that does not require comprehensive IRB review and approval because the only research activity involving the human subjects falls into one or more specific exemption categories as defined by the Common Rule.
Exempt Categories: Education research. Surveys, interviews, educational tests, public observations (that do not involve children) Benign behavioral interventions. Analysis of previously-collected, identifiable info/specimens. Federal research/demonstration projects. Taste and food evaluation studies.
Examples of Commonly Exempted Research Research on educational practices or educational curriculums. Benign behavioral interventions with adult subjects. Anonymous surveys or interviews on non-sensitive topics. Passive observation of public behavior without collection of identifiers.
Research can qualify for an exemption if it is no more than minimal risk and all of the research procedures fit within one or more of the exemption categories in the federal IRB regulations. Studies that qualify for exemption must be submitted to the IRB for review before starting the research.
Yes. If you are gathering data from people and you plan to publish your findings, you absolutely need to go through IRB. Even for things that don't strictly need IRB approval, journals are still going to want to see that an IRB officially declared your research to be ``exempt.''

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The Summary or Annual Report for Non-Exempt Research is a document that outlines the activities and findings of research projects that do not qualify for exemptions under federal regulations. This report ensures compliance with regulatory standards and provides transparency regarding the research conducted.
Researchers and institutions that conduct non-exempt research involving human subjects are required to file the Summary or Annual Report. This includes academic institutions, private organizations, and any entity receiving federal funding for research.
To fill out the Summary or Annual Report, researchers should gather relevant data on their research activities, including participant demographics, methodologies used, outcomes, and any adverse events. They will need to complete the designated form provided by the overseeing regulatory body or institution, ensuring all sections are accurately filled out and supported by documentation.
The purpose of the Summary or Annual Report is to provide oversight and accountability for research involving human subjects, ensure compliance with ethical standards, and facilitate communication between researchers and regulatory authorities regarding research practices and outcomes.
The report must include information such as the title of the research project, the names of the principal investigators, the objectives of the research, the number of participants, a summary of findings, any ethical concerns or issues encountered, and plans for future research. Additionally, any adverse events or unanticipated problems must also be reported.
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