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Emory IRB GuidanceData Safety Monitoring Plans and Data Safety Monitoring Boards What is a DUMP? What are the essential elements of the DUMP? Examples of Dumps elements What is a DSM? What is the
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How to fill out emory irb guidance

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01
To fill out Emory IRB guidance, first, identify if your research involves human subjects. Emory IRB (Institutional Review Board) provides guidance on conducting research that involves human participants to ensure ethical considerations are met.
02
Determine the level of review required for your study. Emory IRB categorizes studies into three levels: Exempt, Expedited, and Full Board. Exempt studies have minimal risk, Expedited studies involve minimal risk but require IRB review, and Full Board studies carry greater risk or involve vulnerable populations.
03
Access the Emory IRB guidance materials. Visit the Emory IRB website to find the necessary forms, templates, and instructions for submitting your research proposal. Familiarize yourself with the specific guidelines provided by Emory IRB.
04
Complete the appropriate application form. Based on the level of review determined for your study, fill out the corresponding application form accurately and thoroughly. Provide clear and concise responses to each question, ensuring all required information is included.
05
Prepare supporting documents. Depending on the nature of your research, Emory IRB may request additional documentation such as consent forms, survey questionnaires, recruitment materials, or data management plans. Ensure these documents align with the ethical principles outlined by the IRB.
06
Submit your application. Follow the submission instructions provided by Emory IRB for electronic or physical submissions. Ensure all required forms, supporting documents, and signatures are included before submitting your application.
07
Await review and feedback. Emory IRB will review your application carefully to assess the ethical implications of your research. They may provide recommendations, seek clarifications, or request modifications to ensure participant protection and adherence to ethical guidelines.
08
Address any requested revisions. If Emory IRB requests modifications to your application or supporting documents, address their concerns promptly and comprehensively. Make the necessary changes and resubmit the revised materials within the given timeframe.
09
Obtain approval or exemption. Once Emory IRB determines that your research meets the necessary ethical standards, you will receive either approval or exemption. Approval indicates that your study can proceed as proposed, while exemption implies that your research poses minimal risk and may not require further IRB oversight.
10
Maintain compliance. Throughout your research project, ensure ongoing compliance with Emory IRB guidance and any specific conditions outlined in your approval. Report any changes to the study design, protocols, or participant information promptly to the IRB to ensure ongoing ethical practices.

Who needs Emory IRB guidance?

Researchers conducting studies involving human subjects, particularly at Emory University, need Emory IRB guidance. This includes faculty, staff, students, and collaborating researchers who are planning to engage in research activities that involve direct interaction or data collection from human participants. The Emory IRB guidance ensures that all individuals conducting research that involves human subjects follow ethical principles and guidelines to protect the rights, welfare, and privacy of the participants. It is essential to consult and seek guidance from Emory IRB to ensure compliance with ethical standards and regulatory requirements.
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Emory IRB guidance refers to the set of rules and instructions provided by Emory University's Institutional Review Board for conducting research involving human subjects.
Researchers, scientists, and any individuals conducting research involving human subjects are required to file Emory IRB guidance.
Emory IRB guidance can be filled out by following the instructions provided by the Institutional Review Board, which may include submitting forms, protocols, and other necessary documentation.
The purpose of Emory IRB guidance is to ensure that research involving human subjects is conducted ethically and in compliance with federal regulations to protect the rights and welfare of research participants.
Emory IRB guidance typically requires information such as the study protocol, informed consent forms, risks and benefits to participants, and details on how participant confidentiality will be maintained.
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