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EIRE Protocol Template (Version 1.7) 1.0General Information×Please enter the full title of your study: Randomized Controlled Trial Comparing plus Omeprazole with alone in Eosinophilic Esophagitis
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Step 1: Open the EIRB protocol template version.
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Step 2: Fill in the required information in the designated fields, such as project title, investigator names, and contact information.
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Step 3: Provide a clear and concise project summary, outlining the objectives, methods, and expected outcomes.
04
Step 4: Describe the study population and inclusion/exclusion criteria, if applicable.
05
Step 5: Provide a detailed description of the proposed interventions, procedures, or experiments.
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Step 6: Include any necessary documentation, such as informed consent forms or study materials.
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Step 7: Clearly define the risks and potential benefits for participants.
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Step 8: Discuss the data collection and analysis plan in a step-by-step manner.
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Step 9: Address any potential ethical concerns and provide an explanation of how they will be mitigated.
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Step 10: Review and revise the completed EIRB protocol template version for accuracy and completeness.
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Step 11: Submit the filled-out EIRB protocol template version to the relevant authority or committee for review and approval.
Who needs eirb protocol template version?
01
Researchers conducting studies involving human subjects.
02
Institutions or organizations requiring ethics review and approval for research projects.
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What is eirb protocol template version?
The eirb protocol template version is a standardized format for documenting research protocols.
Who is required to file eirb protocol template version?
Researchers conducting studies that involve human subjects are required to file the eirb protocol template version.
How to fill out eirb protocol template version?
Researchers must provide detailed information about their study design, methods, risks, and benefits in the eirb protocol template version.
What is the purpose of eirb protocol template version?
The eirb protocol template version is designed to ensure that research involving human subjects is ethical and follows best practices.
What information must be reported on eirb protocol template version?
Researchers must report information such as study objectives, participant inclusion criteria, data collection methods, and potential risks to participants.
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